MOXD1 (monooxygenase DBH like 1) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: MOXD1 (monooxygenase DBH like 1) Homo sapiens
Analyze
Symbol: MOXD1
Name: monooxygenase DBH like 1
RGD ID: 1320700
HGNC Page HGNC:21063
Description: Predicted to enable copper ion binding activity and dopamine beta-monooxygenase activity. Predicted to be involved in dopamine catabolic process; norepinephrine biosynthetic process; and octopamine biosynthetic process. Part of endoplasmic reticulum membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: DBH-like monooxygenase protein 1; dJ248E1.1; DKFZp564G202; dopamine-oxygenase; monooxygenase X; monooxygenase, DBH-like 1; MOX; PRO5780
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386132,296,055 - 132,401,475 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6132,296,055 - 132,401,475 (-)EnsemblGRCh38hg38GRCh38
GRCh376132,617,194 - 132,722,614 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366132,658,887 - 132,764,357 (-)NCBINCBI36Build 36hg18NCBI36
Build 346132,658,900 - 132,737,897NCBI
Celera6133,364,075 - 133,469,523 (-)NCBICelera
Cytogenetic Map6q23.2NCBI
HuRef6130,192,320 - 130,297,382 (-)NCBIHuRef
CHM1_16132,880,907 - 132,986,340 (-)NCBICHM1_1
T2T-CHM13v2.06133,491,085 - 133,596,511 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View
silicosis  (EXP)

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(1->4)-beta-D-glucan  (ISO)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
2-bromohexadecanoic acid  (EXP)
4,4'-sulfonyldiphenol  (ISO)
6-propyl-2-thiouracil  (ISO)
8-Br-cAMP  (EXP)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (EXP,ISO)
alpha-Zearalanol  (ISO)
aristolochic acid A  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
arsenite(3-)  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[b]fluoranthene  (ISO)
Benzo[k]fluoranthene  (ISO)
bis(2-ethylhexyl) phthalate  (ISO)
bisphenol A  (ISO)
bisphenol F  (ISO)
butanal  (EXP)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
carbamazepine  (EXP)
CGP 52608  (EXP)
chromium(6+)  (ISO)
cisplatin  (EXP)
Cuprizon  (ISO)
diazinon  (EXP)
dichloroacetic acid  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
epoxiconazole  (ISO)
fenvalerate  (ISO)
fonofos  (EXP)
GSK-J4  (EXP)
ivermectin  (EXP)
lipopolysaccharide  (ISO)
manganese atom  (EXP)
manganese(0)  (EXP)
manganese(II) chloride  (EXP)
mono(2-ethylhexyl) phthalate  (ISO)
nickel atom  (EXP)
nickel sulfate  (EXP)
paracetamol  (EXP,ISO)
parathion  (EXP)
pentanal  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
perfluorooctanoic acid  (ISO)
phenobarbital  (ISO)
pirinixic acid  (EXP)
propanal  (EXP)
SB 431542  (EXP)
sodium arsenate  (EXP)
sodium arsenite  (EXP,ISO)
Soman  (ISO)
sulforaphane  (EXP)
terbufos  (EXP)
tert-butyl hydroperoxide  (EXP)
testosterone  (ISO)
thalidomide  (ISO)
tributylstannane  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vitamin E  (EXP)
vorinostat  (EXP)
zinc atom  (ISO)
zinc(0)  (ISO)
zoledronic acid  (EXP)

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9751809   PMID:12477932   PMID:12975309   PMID:15337741   PMID:20581860   PMID:21873635   PMID:21900206   PMID:23251661   PMID:24667918   PMID:25416956   PMID:26186194   PMID:28514442  
PMID:29892012   PMID:30561431   PMID:30585266   PMID:32296183   PMID:32707033   PMID:33853758   PMID:33961781   PMID:34079125   PMID:35271311   PMID:36897256   PMID:37314216   PMID:37499664  
PMID:37616343   PMID:38200441   PMID:38905335  


Genomics

Comparative Map Data
MOXD1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386132,296,055 - 132,401,475 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6132,296,055 - 132,401,475 (-)EnsemblGRCh38hg38GRCh38
GRCh376132,617,194 - 132,722,614 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366132,658,887 - 132,764,357 (-)NCBINCBI36Build 36hg18NCBI36
Build 346132,658,900 - 132,737,897NCBI
Celera6133,364,075 - 133,469,523 (-)NCBICelera
Cytogenetic Map6q23.2NCBI
HuRef6130,192,320 - 130,297,382 (-)NCBIHuRef
CHM1_16132,880,907 - 132,986,340 (-)NCBICHM1_1
T2T-CHM13v2.06133,491,085 - 133,596,511 (-)NCBIT2T-CHM13v2.0
Moxd1
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391024,099,415 - 24,178,681 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1024,099,415 - 24,178,688 (+)EnsemblGRCm39 Ensembl
GRCm381024,223,517 - 24,302,783 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1024,223,517 - 24,302,790 (+)EnsemblGRCm38mm10GRCm38
MGSCv371023,943,323 - 24,022,589 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361023,912,933 - 23,992,199 (+)NCBIMGSCv36mm8
Celera1025,156,513 - 25,235,667 (+)NCBICelera
Cytogenetic Map10A4NCBI
cM Map1011.48NCBI
Moxd1
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8122,894,543 - 22,984,599 (-)NCBIGRCr8
mRatBN7.2121,075,124 - 21,165,348 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl121,075,122 - 21,161,779 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.0122,124,498 - 22,206,565 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl122,124,495 - 22,206,505 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0123,604,654 - 23,686,707 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4121,599,942 - 21,686,543 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1121,603,599 - 21,688,511 (-)NCBI
Celera119,826,681 - 19,913,152 (-)NCBICelera
Cytogenetic Map1p12NCBI
Moxd1
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543612,818,375 - 12,872,396 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495543612,818,375 - 12,872,229 (-)NCBIChiLan1.0ChiLan1.0
MOXD1
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v25152,279,758 - 152,384,060 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan16150,186,825 - 150,291,132 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v06130,073,802 - 130,177,753 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.16134,182,129 - 134,285,995 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl6134,179,412 - 134,285,995 (-)Ensemblpanpan1.1panPan2
MOXD1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1125,018,452 - 25,114,028 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl125,018,509 - 25,112,478 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha126,404,602 - 26,499,087 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0125,328,412 - 25,423,166 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl125,327,253 - 25,423,145 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1125,374,169 - 25,468,891 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0125,271,493 - 25,367,112 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0125,535,032 - 25,630,566 (-)NCBIUU_Cfam_GSD_1.0
Moxd1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404946120,553,333 - 120,634,611 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936560332,718 - 413,559 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936560334,294 - 413,559 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
MOXD1
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl131,282,506 - 31,367,779 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1131,282,491 - 31,367,589 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2134,802,968 - 34,888,612 (+)NCBISscrofa10.2Sscrofa10.2susScr3
MOXD1
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11341,138,661 - 41,271,779 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1341,139,408 - 41,248,665 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604013,329,004 - 13,453,440 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Moxd1
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046247536,377,330 - 6,471,085 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046247536,379,583 - 6,471,020 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in MOXD1
62 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_015529.3(MOXD1):c.664-11078C>T single nucleotide variant Lung cancer [RCV000096531] Chr6:132339672 [GRCh38]
Chr6:132660811 [GRCh37]
Chr6:6q23.2
uncertain significance
GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3 copy number gain See cases [RCV000139729] Chr6:74382807..142040500 [GRCh38]
Chr6:75092523..142361637 [GRCh37]
Chr6:75149243..142403330 [NCBI36]
Chr6:6q13-24.1
pathogenic
GRCh38/hg38 6q22.32-23.2(chr6:126494533-132497855)x1 copy number loss See cases [RCV000142805] Chr6:126494533..132497855 [GRCh38]
Chr6:126815679..132818994 [GRCh37]
Chr6:126857372..132860687 [NCBI36]
Chr6:6q22.32-23.2
likely pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27
pathogenic
NM_015529.4(MOXD1):c.1337A>G (p.Asn446Ser) single nucleotide variant not specified [RCV004326966] Chr6:132320657 [GRCh38]
Chr6:132641796 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.703C>T (p.His235Tyr) single nucleotide variant not specified [RCV004304591] Chr6:132328555 [GRCh38]
Chr6:132649694 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1477A>T (p.Ile493Phe) single nucleotide variant not specified [RCV004317574] Chr6:132315666 [GRCh38]
Chr6:132636805 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1693G>T (p.Ala565Ser) single nucleotide variant not specified [RCV004310075] Chr6:132297302 [GRCh38]
Chr6:132618441 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1397T>A (p.Leu466His) single nucleotide variant not specified [RCV004327071] Chr6:132315746 [GRCh38]
Chr6:132636885 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.55G>T (p.Gly19Trp) single nucleotide variant not specified [RCV004281893] Chr6:132401372 [GRCh38]
Chr6:132722511 [GRCh37]
Chr6:6q23.2
uncertain significance
GRCh37/hg19 6q23.2-23.3(chr6:131388023-137469640)x1 copy number loss not provided [RCV000682724] Chr6:131388023..137469640 [GRCh37]
Chr6:6q23.2-23.3
pathogenic
GRCh37/hg19 6q23.2-23.3(chr6:132002460-137160850)x1 copy number loss not provided [RCV000682725] Chr6:132002460..137160850 [GRCh37]
Chr6:6q23.2-23.3
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27
pathogenic
GRCh37/hg19 6q23.2(chr6:132702249-132712307)x1 copy number loss not provided [RCV000746038] Chr6:132702249..132712307 [GRCh37]
Chr6:6q23.2
benign
GRCh37/hg19 6q22.33-23.2(chr6:129513837-132618991) copy number loss not provided [RCV000767715] Chr6:129513837..132618991 [GRCh37]
Chr6:6q22.33-23.2
likely pathogenic
GRCh37/hg19 6q23.2(chr6:131673206-132706248)x1 copy number loss not provided [RCV000848451] Chr6:131673206..132706248 [GRCh37]
Chr6:6q23.2
uncertain significance
Single allele deletion Interstitial 6q microdeletion syndrome [RCV002280353] Chr6:115941808..133892653 [GRCh38]
Chr6:6q22.1-23.2
pathogenic
GRCh37/hg19 6q23.1-23.3(chr6:130769034-136009217)x1 copy number loss not provided [RCV001829086] Chr6:130769034..136009217 [GRCh37]
Chr6:6q23.1-23.3
pathogenic
NM_015529.4(MOXD1):c.1064T>C (p.Met355Thr) single nucleotide variant not specified [RCV004327009] Chr6:132323980 [GRCh38]
Chr6:132645119 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1552C>T (p.Leu518Phe) single nucleotide variant not specified [RCV004156304] Chr6:132297912 [GRCh38]
Chr6:132619051 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.100G>A (p.Glu34Lys) single nucleotide variant not specified [RCV004146947] Chr6:132401327 [GRCh38]
Chr6:132722466 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1433C>T (p.Thr478Ile) single nucleotide variant not specified [RCV004106214] Chr6:132315710 [GRCh38]
Chr6:132636849 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.281C>T (p.Ala94Val) single nucleotide variant not specified [RCV004144676] Chr6:132374761 [GRCh38]
Chr6:132695900 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1093A>T (p.Thr365Ser) single nucleotide variant not specified [RCV004139607] Chr6:132323951 [GRCh38]
Chr6:132645090 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.593A>G (p.Asn198Ser) single nucleotide variant not specified [RCV004225268] Chr6:132372678 [GRCh38]
Chr6:132693817 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.650A>G (p.His217Arg) single nucleotide variant not specified [RCV004101694] Chr6:132372621 [GRCh38]
Chr6:132693760 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.747C>A (p.Ser249Arg) single nucleotide variant not specified [RCV004232621] Chr6:132328511 [GRCh38]
Chr6:132649650 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1405C>A (p.Leu469Ile) single nucleotide variant not specified [RCV004130467] Chr6:132315738 [GRCh38]
Chr6:132636877 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.376C>A (p.Leu126Met) single nucleotide variant not specified [RCV004158966] Chr6:132374666 [GRCh38]
Chr6:132695805 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1820C>T (p.Thr607Met) single nucleotide variant not specified [RCV004071346] Chr6:132297175 [GRCh38]
Chr6:132618314 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1259A>G (p.Asn420Ser) single nucleotide variant not specified [RCV004170980] Chr6:132322725 [GRCh38]
Chr6:132643864 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.59G>A (p.Gly20Asp) single nucleotide variant not specified [RCV004081241] Chr6:132401368 [GRCh38]
Chr6:132722507 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.37C>T (p.Leu13Phe) single nucleotide variant not specified [RCV004174659] Chr6:132401390 [GRCh38]
Chr6:132722529 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1057C>T (p.Pro353Ser) single nucleotide variant not specified [RCV004223427] Chr6:132323987 [GRCh38]
Chr6:132645126 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.832A>G (p.Ile278Val) single nucleotide variant not specified [RCV004338823] Chr6:132328426 [GRCh38]
Chr6:132649565 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1421G>T (p.Arg474Ile) single nucleotide variant not specified [RCV004336728] Chr6:132315722 [GRCh38]
Chr6:132636861 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1501C>A (p.Pro501Thr) single nucleotide variant not specified [RCV004359257] Chr6:132315642 [GRCh38]
Chr6:132636781 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1250T>C (p.Phe417Ser) single nucleotide variant not specified [RCV004352397] Chr6:132322734 [GRCh38]
Chr6:132643873 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1330C>T (p.Arg444Cys) single nucleotide variant not specified [RCV004334828] Chr6:132320664 [GRCh38]
Chr6:132641803 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1376G>A (p.Ser459Asn) single nucleotide variant not specified [RCV004336744] Chr6:132315767 [GRCh38]
Chr6:132636906 [GRCh37]
Chr6:6q23.2
uncertain significance
GRCh37/hg19 6q22.31-23.3(chr6:120218852-137160850)x1 copy number loss not provided [RCV003482930] Chr6:120218852..137160850 [GRCh37]
Chr6:6q22.31-23.3
pathogenic
GRCh37/hg19 6q23.2-24.2(chr6:131569837-145572239)x3 copy number gain not specified [RCV003986663] Chr6:131569837..145572239 [GRCh37]
Chr6:6q23.2-24.2
pathogenic
GRCh37/hg19 6q22.31-25.3(chr6:119840686-156623091)x3 copy number gain not specified [RCV003986631] Chr6:119840686..156623091 [GRCh37]
Chr6:6q22.31-25.3
pathogenic
NM_015529.4(MOXD1):c.1106T>C (p.Leu369Pro) single nucleotide variant not specified [RCV004487863] Chr6:132323938 [GRCh38]
Chr6:132645077 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1198C>A (p.Arg400Ser) single nucleotide variant not specified [RCV004487872] Chr6:132322786 [GRCh38]
Chr6:132643925 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1231C>T (p.Leu411Phe) single nucleotide variant not specified [RCV004487880] Chr6:132322753 [GRCh38]
Chr6:132643892 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1208G>A (p.Arg403Gln) single nucleotide variant not specified [RCV004487876] Chr6:132322776 [GRCh38]
Chr6:132643915 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.137G>A (p.Ser46Asn) single nucleotide variant not specified [RCV004487890] Chr6:132401290 [GRCh38]
Chr6:132722429 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1676C>T (p.Ser559Leu) single nucleotide variant not specified [RCV004487909] Chr6:132297788 [GRCh38]
Chr6:132618927 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.86C>A (p.Thr29Asn) single nucleotide variant not specified [RCV004487953] Chr6:132401341 [GRCh38]
Chr6:132722480 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.380A>G (p.His127Arg) single nucleotide variant not specified [RCV004487924] Chr6:132374662 [GRCh38]
Chr6:132695801 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1146T>A (p.His382Gln) single nucleotide variant not specified [RCV004487867] Chr6:132322838 [GRCh38]
Chr6:132643977 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.133G>C (p.Gly45Arg) single nucleotide variant not specified [RCV004487888] Chr6:132401294 [GRCh38]
Chr6:132722433 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1009G>C (p.Gly337Arg) single nucleotide variant not specified [RCV004495862] Chr6:132324035 [GRCh38]
Chr6:132645174 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.200C>G (p.Thr67Ser) single nucleotide variant not specified [RCV004643389] Chr6:132401227 [GRCh38]
Chr6:132722366 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.758C>T (p.Ser253Phe) single nucleotide variant not specified [RCV004643388] Chr6:132328500 [GRCh38]
Chr6:132649639 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.760G>A (p.Gly254Ser) single nucleotide variant not specified [RCV004643387] Chr6:132328498 [GRCh38]
Chr6:132649637 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.923A>T (p.Tyr308Phe) single nucleotide variant not specified [RCV004643390] Chr6:132328036 [GRCh38]
Chr6:132649175 [GRCh37]
Chr6:6q23.2
uncertain significance
NC_000006.11:g.(?_131894423)_(133849943_?)del deletion not provided [RCV004578838] Chr6:131894423..133849943 [GRCh37]
Chr6:6q23.2
pathogenic
NM_015529.4(MOXD1):c.1417C>T (p.Pro473Ser) single nucleotide variant not specified [RCV004629074] Chr6:132315726 [GRCh38]
Chr6:132636865 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1445G>C (p.Ser482Thr) single nucleotide variant not specified [RCV004824701] Chr6:132315698 [GRCh38]
Chr6:132636837 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.707A>G (p.His236Arg) single nucleotide variant not specified [RCV004828439] Chr6:132328551 [GRCh38]
Chr6:132649690 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.300A>T (p.Lys100Asn) single nucleotide variant not specified [RCV004828440] Chr6:132374742 [GRCh38]
Chr6:132695881 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1263C>G (p.Phe421Leu) single nucleotide variant not specified [RCV004828429] Chr6:132322721 [GRCh38]
Chr6:132643860 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1340C>T (p.Thr447Met) single nucleotide variant not specified [RCV004828432] Chr6:132320654 [GRCh38]
Chr6:132641793 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.161T>G (p.Val54Gly) single nucleotide variant not specified [RCV004828438] Chr6:132401266 [GRCh38]
Chr6:132722405 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1291C>A (p.Gln431Lys) single nucleotide variant not specified [RCV004828433] Chr6:132322693 [GRCh38]
Chr6:132643832 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1601G>A (p.Gly534Asp) single nucleotide variant not specified [RCV004828437] Chr6:132297863 [GRCh38]
Chr6:132619002 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1286A>G (p.Glu429Gly) single nucleotide variant not specified [RCV004824702] Chr6:132322698 [GRCh38]
Chr6:132643837 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.410C>T (p.Thr137Met) single nucleotide variant not specified [RCV004828430] Chr6:132374632 [GRCh38]
Chr6:132695771 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1187G>A (p.Gly396Asp) single nucleotide variant not specified [RCV004828431] Chr6:132322797 [GRCh38]
Chr6:132643936 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.145G>T (p.Ala49Ser) single nucleotide variant not specified [RCV004828434] Chr6:132401282 [GRCh38]
Chr6:132722421 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.1222A>G (p.Met408Val) single nucleotide variant not specified [RCV004828435] Chr6:132322762 [GRCh38]
Chr6:132643901 [GRCh37]
Chr6:6q23.2
uncertain significance
NM_015529.4(MOXD1):c.956A>G (p.Asp319Gly) single nucleotide variant not specified [RCV004828436] Chr6:132324088 [GRCh38]
Chr6:132645227 [GRCh37]
Chr6:6q23.2
uncertain significance
miRNA Target Status (No longer updated)

Predicted Target Of
Summary Value
Count of predictions:1533
Count of miRNA genes:713
Interacting mature miRNAs:805
Transcripts:ENST00000336749, ENST00000367963, ENST00000392401, ENST00000489128
Prediction methods:Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
407028931GWAS677907_Hlean body mass QTL GWAS677907 (human)0.0000001body lean mass (VT:0010483)total body lean mass (CMO:0003950)6132321978132321979Human
407043637GWAS692613_Hbody weight QTL GWAS692613 (human)0.000009body mass (VT:0001259)body weight (CMO:0000012)6132321978132321979Human
407046333GWAS695309_Henergy expenditure QTL GWAS695309 (human)0.000001energy expenditure trait (VT:0005450)6132321978132321979Human
597336629GWAS1432703_HRS-10-hydroxywarfarin to RS-warfarin ratio measurement QTL GWAS1432703 (human)0.000009RS-10-hydroxywarfarin to RS-warfarin ratio measurement6132300181132300182Human
407042717GWAS691693_Hmaximal oxygen uptake measurement QTL GWAS691693 (human)0.000002energy expenditure trait (VT:0005450)maximal oxygen consumption (CMO:0000135)6132321978132321979Human

Markers in Region
D6S413  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,053 - 132,646,240UniSTSGRCh37
GRCh376132,646,061 - 132,646,224UniSTSGRCh37
GRCh376132,646,119 - 132,646,224UniSTSGRCh37
Build 366132,687,746 - 132,687,933RGDNCBI36
Celera6133,392,936 - 133,393,125RGD
Celera6133,393,004 - 133,393,109UniSTS
Celera6133,392,944 - 133,393,109UniSTS
Cytogenetic Map6q23.2UniSTS
HuRef6130,221,215 - 130,221,320UniSTS
HuRef6130,221,155 - 130,221,320UniSTS
HuRef6130,221,147 - 130,221,336UniSTS
Marshfield Genetic Map6131.07RGD
Genethon Genetic Map6131.5UniSTS
deCODE Assembly Map6131.33UniSTS
Stanford-G3 RH Map65447.0UniSTS
GeneMap99-GB4 RH Map6532.92UniSTS
Whitehead-RH Map6756.1UniSTS
Whitehead-YAC Contig Map6 UniSTS
NCBI RH Map61529.3UniSTS
GeneMap99-G3 RH Map65750.0UniSTS
NIB446  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,617,261 - 132,617,418UniSTSGRCh37
Build 366132,658,954 - 132,659,111RGDNCBI36
Celera6133,364,142 - 133,364,299RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,387 - 130,192,544UniSTS
GeneMap99-GB4 RH Map6532.92UniSTS
Whitehead-RH Map6756.1UniSTS
NCBI RH Map61538.9UniSTS
RH45731  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,617,371 - 132,617,490UniSTSGRCh37
Build 366132,659,064 - 132,659,183RGDNCBI36
Celera6133,364,252 - 133,364,371RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,497 - 130,192,616UniSTS
GeneMap99-GB4 RH Map6532.92UniSTS
NCBI RH Map61538.9UniSTS
RH79871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,617,236 - 132,617,438UniSTSGRCh37
Build 366132,658,929 - 132,659,131RGDNCBI36
Celera6133,364,117 - 133,364,319RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,362 - 130,192,564UniSTS
RH119733  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,618,061 - 132,618,258UniSTSGRCh37
Build 366132,659,754 - 132,659,951RGDNCBI36
Celera6133,364,942 - 133,365,139RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,193,187 - 130,193,384UniSTS
TNG Radiation Hybrid Map665790.0UniSTS
SHGC-132284  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,022 - 132,646,238UniSTSGRCh37
Build 366132,687,715 - 132,687,931RGDNCBI36
Celera6133,392,905 - 133,393,123RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,221,116 - 130,221,334UniSTS
TNG Radiation Hybrid Map665739.0UniSTS
TNG Radiation Hybrid Map665776.0UniSTS
ECD00112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,655,482 - 132,656,416UniSTSGRCh37
Build 366132,697,175 - 132,698,109RGDNCBI36
Celera6133,402,367 - 133,403,301RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,230,588 - 130,231,522UniSTS
ECD00652  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,642,425 - 132,643,320UniSTSGRCh37
Build 366132,684,118 - 132,685,013RGDNCBI36
Celera6133,389,308 - 133,390,203RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,217,519 - 130,218,414UniSTS
ECD01247  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,643,466 - 132,644,337UniSTSGRCh37
Build 366132,685,159 - 132,686,030RGDNCBI36
Celera6133,390,349 - 133,391,220RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,218,560 - 130,219,431UniSTS
ECD04062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,660,169 - 132,660,944UniSTSGRCh37
Build 366132,701,862 - 132,702,637RGDNCBI36
Celera6133,407,054 - 133,407,829RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,235,275 - 130,236,050UniSTS
ECD04903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,617,732 - 132,618,482UniSTSGRCh37
Build 366132,659,425 - 132,660,175RGDNCBI36
Celera6133,364,613 - 133,365,363RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,858 - 130,193,608UniSTS
ECD05328  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,649,350 - 132,650,088UniSTSGRCh37
Build 366132,691,043 - 132,691,781RGDNCBI36
Celera6133,396,235 - 133,396,973RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,224,446 - 130,225,184UniSTS
ECD06401  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,654,499 - 132,655,208UniSTSGRCh37
Build 366132,696,192 - 132,696,901RGDNCBI36
Celera6133,401,384 - 133,402,093RGD
Cytogenetic Map6q23.2UniSTS
ECD06584  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,621,609 - 132,622,313UniSTSGRCh37
Build 366132,663,302 - 132,664,006RGDNCBI36
Celera6133,368,490 - 133,369,194RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,196,735 - 130,197,439UniSTS
ECD06669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,641,384 - 132,642,086UniSTSGRCh37
Build 366132,683,077 - 132,683,779RGDNCBI36
Celera6133,388,267 - 133,388,969RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,216,478 - 130,217,180UniSTS
ECD08114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,667,426 - 132,668,089UniSTSGRCh37
Build 366132,709,119 - 132,709,782RGDNCBI36
Celera6133,414,310 - 133,414,973RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,242,530 - 130,243,193UniSTS
ECD08180  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,618,522 - 132,619,183UniSTSGRCh37
Build 366132,660,215 - 132,660,876RGDNCBI36
Celera6133,365,403 - 133,366,064RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,193,648 - 130,194,309UniSTS
ECD08221  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,656,936 - 132,657,596UniSTSGRCh37
Build 366132,698,629 - 132,699,289RGDNCBI36
Celera6133,403,821 - 133,404,481RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,232,042 - 130,232,702UniSTS
ECD08715  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,650,632 - 132,651,279UniSTSGRCh37
Build 366132,692,325 - 132,692,972RGDNCBI36
Celera6133,397,517 - 133,398,164RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,225,728 - 130,226,375UniSTS
ECD08788  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,657,622 - 132,658,267UniSTSGRCh37
Build 366132,699,315 - 132,699,960RGDNCBI36
Celera6133,404,507 - 133,405,152RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,232,728 - 130,233,373UniSTS
ECD08955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,658,441 - 132,659,081UniSTSGRCh37
Build 366132,700,134 - 132,700,774RGDNCBI36
Celera6133,405,326 - 133,405,966RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,233,547 - 130,234,187UniSTS
ECD09479  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,648,687 - 132,649,314UniSTSGRCh37
Build 366132,690,380 - 132,691,007RGDNCBI36
Celera6133,395,572 - 133,396,199RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,223,783 - 130,224,410UniSTS
ECD09964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,636,626 - 132,637,240UniSTSGRCh37
Build 366132,678,319 - 132,678,933RGDNCBI36
Celera6133,383,508 - 133,384,122RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,211,720 - 130,212,334UniSTS
ECD10372  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,663,630 - 132,664,233UniSTSGRCh37
Build 366132,705,323 - 132,705,926RGDNCBI36
Celera6133,410,514 - 133,411,117RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,238,734 - 130,239,337UniSTS
ECD10484  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,668,853 - 132,669,453UniSTSGRCh37
Build 366132,710,546 - 132,711,146RGDNCBI36
Celera6133,415,738 - 133,416,338RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,243,957 - 130,244,557UniSTS
ECD11005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,669,502 - 132,670,086UniSTSGRCh37
Build 366132,711,195 - 132,711,779RGDNCBI36
Celera6133,416,387 - 133,416,971RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,244,606 - 130,245,190UniSTS
ECD11293  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,617,085 - 132,617,661UniSTSGRCh37
Build 366132,658,778 - 132,659,354RGDNCBI36
Celera6133,363,966 - 133,364,542RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,211 - 130,192,787UniSTS
ECD11694  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,652,964 - 132,653,528UniSTSGRCh37
Build 366132,694,657 - 132,695,221RGDNCBI36
Celera6133,399,849 - 133,400,413RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,228,060 - 130,228,624UniSTS
ECD12291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,633,079 - 132,633,626UniSTSGRCh37
Build 366132,674,772 - 132,675,319RGDNCBI36
Celera6133,379,961 - 133,380,508RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,208,173 - 130,208,720UniSTS
ECD13553  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,644,669 - 132,645,183UniSTSGRCh37
Build 366132,686,362 - 132,686,876RGDNCBI36
Celera6133,391,552 - 133,392,066RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,219,763 - 130,220,277UniSTS
ECD14474  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,666,772 - 132,667,264UniSTSGRCh37
Build 366132,708,465 - 132,708,957RGDNCBI36
Celera6133,413,656 - 133,414,148RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,241,876 - 130,242,368UniSTS
ECD14883  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,652,210 - 132,652,693UniSTSGRCh37
Build 366132,693,903 - 132,694,386RGDNCBI36
Celera6133,399,095 - 133,399,578RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,227,306 - 130,227,789UniSTS
ECD15589  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,651,697 - 132,652,163UniSTSGRCh37
Build 366132,693,390 - 132,693,856RGDNCBI36
Celera6133,398,582 - 133,399,048RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,226,793 - 130,227,259UniSTS
ECD16340  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,653,666 - 132,654,110UniSTSGRCh37
Build 366132,695,359 - 132,695,803RGDNCBI36
Celera6133,400,551 - 133,400,995RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,228,762 - 130,229,206UniSTS
ECD17384  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,662,589 - 132,662,989UniSTSGRCh37
Build 366132,704,282 - 132,704,682RGDNCBI36
Celera6133,409,473 - 133,409,873RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,237,695 - 130,238,093UniSTS
ECD17485  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,633,765 - 132,634,161UniSTSGRCh37
Build 366132,675,458 - 132,675,854RGDNCBI36
Celera6133,380,647 - 133,381,043RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,208,859 - 130,209,255UniSTS
ECD18572  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,622,471 - 132,622,825UniSTSGRCh37
Build 366132,664,164 - 132,664,518RGDNCBI36
Celera6133,369,352 - 133,369,706RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,197,595 - 130,197,949UniSTS
ECD19291  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,645,359 - 132,645,685UniSTSGRCh37
Build 366132,687,052 - 132,687,378RGDNCBI36
Celera6133,392,242 - 133,392,568RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,220,453 - 130,220,779UniSTS
ECD20157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,971 - 132,647,265UniSTSGRCh37
Build 366132,688,664 - 132,688,958RGDNCBI36
Celera6133,393,856 - 133,394,150RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,222,067 - 130,222,361UniSTS
ECD20230  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,620,637 - 132,620,928UniSTSGRCh37
Build 366132,662,330 - 132,662,621RGDNCBI36
Celera6133,367,518 - 133,367,809RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,195,763 - 130,196,054UniSTS
ECD20311  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,621,058 - 132,621,346UniSTSGRCh37
Build 366132,662,751 - 132,663,039RGDNCBI36
Celera6133,367,939 - 133,368,227RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,196,184 - 130,196,472UniSTS
ECD20735  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,623,210 - 132,623,483UniSTSGRCh37
Build 366132,664,903 - 132,665,176RGDNCBI36
Celera6133,370,091 - 133,370,364RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,198,334 - 130,198,607UniSTS
ECD21119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,664,995 - 132,665,255UniSTSGRCh37
Build 366132,706,688 - 132,706,948RGDNCBI36
Celera6133,411,879 - 133,412,139RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,240,099 - 130,240,359UniSTS
ECD22510  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,661,334 - 132,661,550UniSTSGRCh37
Build 366132,703,027 - 132,703,243RGDNCBI36
Celera6133,408,219 - 133,408,435RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,236,440 - 130,236,656UniSTS
ECD22649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,619,485 - 132,619,697UniSTSGRCh37
Build 366132,661,178 - 132,661,390RGDNCBI36
Celera6133,366,366 - 133,366,578RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,194,611 - 130,194,823UniSTS
ECD22868  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,659,408 - 132,659,613UniSTSGRCh37
Build 366132,701,101 - 132,701,306RGDNCBI36
Celera6133,406,293 - 133,406,498RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,234,514 - 130,234,719UniSTS
ECD23777  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,634,545 - 132,634,721UniSTSGRCh37
Build 366132,676,238 - 132,676,414RGDNCBI36
Celera6133,381,427 - 133,381,603RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,209,639 - 130,209,815UniSTS
ECD24393  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,203 - 132,646,336UniSTSGRCh37
Build 366132,687,896 - 132,688,029RGDNCBI36
Celera6133,393,088 - 133,393,221RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,221,299 - 130,221,432UniSTS
ECD24533  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,645,879 - 132,645,981UniSTSGRCh37
Build 366132,687,572 - 132,687,674RGDNCBI36
Celera6133,392,762 - 133,392,864RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,220,973 - 130,221,075UniSTS
REN30900  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,616,893 - 132,617,133UniSTSGRCh37
Build 366132,658,586 - 132,658,826RGDNCBI36
Celera6133,363,774 - 133,364,014RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,019 - 130,192,259UniSTS
REN30901  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,617,091 - 132,617,329UniSTSGRCh37
Build 366132,658,784 - 132,659,022RGDNCBI36
Celera6133,363,972 - 133,364,210RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,217 - 130,192,455UniSTS
REN30902  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,617,299 - 132,617,558UniSTSGRCh37
Build 366132,658,992 - 132,659,251RGDNCBI36
Celera6133,364,180 - 133,364,439RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,425 - 130,192,684UniSTS
REN30903  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,617,534 - 132,617,779UniSTSGRCh37
Build 366132,659,227 - 132,659,472RGDNCBI36
Celera6133,364,415 - 133,364,660RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,660 - 130,192,905UniSTS
REN30904  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,617,765 - 132,618,010UniSTSGRCh37
Build 366132,659,458 - 132,659,703RGDNCBI36
Celera6133,364,646 - 133,364,891RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,192,891 - 130,193,136UniSTS
REN30905  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,618,006 - 132,618,231UniSTSGRCh37
Build 366132,659,699 - 132,659,924RGDNCBI36
Celera6133,364,887 - 133,365,112RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,193,132 - 130,193,357UniSTS
REN30906  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,618,208 - 132,618,461UniSTSGRCh37
Build 366132,659,901 - 132,660,154RGDNCBI36
Celera6133,365,089 - 133,365,342RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,193,334 - 130,193,587UniSTS
REN30907  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,618,455 - 132,618,679UniSTSGRCh37
Build 366132,660,148 - 132,660,372RGDNCBI36
Celera6133,365,336 - 133,365,560RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,193,581 - 130,193,805UniSTS
REN30908  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,618,656 - 132,618,907UniSTSGRCh37
Build 366132,660,349 - 132,660,600RGDNCBI36
Celera6133,365,537 - 133,365,788RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,193,782 - 130,194,033UniSTS
REN30909  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,618,892 - 132,619,149UniSTSGRCh37
Build 366132,660,585 - 132,660,842RGDNCBI36
Celera6133,365,773 - 133,366,030RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,194,018 - 130,194,275UniSTS
REN30910  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,619,071 - 132,619,323UniSTSGRCh37
Build 366132,660,764 - 132,661,016RGDNCBI36
Celera6133,365,952 - 133,366,204RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,194,197 - 130,194,449UniSTS
REN30911  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,619,293 - 132,619,519UniSTSGRCh37
Build 366132,660,986 - 132,661,212RGDNCBI36
Celera6133,366,174 - 133,366,400RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,194,419 - 130,194,645UniSTS
REN30912  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,619,484 - 132,619,746UniSTSGRCh37
Build 366132,661,177 - 132,661,439RGDNCBI36
Celera6133,366,365 - 133,366,627RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,194,610 - 130,194,872UniSTS
REN30913  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,619,696 - 132,619,929UniSTSGRCh37
Build 366132,661,389 - 132,661,622RGDNCBI36
Celera6133,366,577 - 133,366,810RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,194,822 - 130,195,055UniSTS
REN30914  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,619,923 - 132,620,185UniSTSGRCh37
Build 366132,661,616 - 132,661,878RGDNCBI36
Celera6133,366,804 - 133,367,066RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,195,049 - 130,195,311UniSTS
REN30915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,620,164 - 132,620,431UniSTSGRCh37
Build 366132,661,857 - 132,662,124RGDNCBI36
Celera6133,367,045 - 133,367,312RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,195,290 - 130,195,557UniSTS
REN30916  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,620,418 - 132,620,673UniSTSGRCh37
Build 366132,662,111 - 132,662,366RGDNCBI36
Celera6133,367,299 - 133,367,554RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,195,544 - 130,195,799UniSTS
REN30917  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,620,650 - 132,620,900UniSTSGRCh37
Build 366132,662,343 - 132,662,593RGDNCBI36
Celera6133,367,531 - 133,367,781RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,195,776 - 130,196,026UniSTS
REN30918  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,620,870 - 132,621,094UniSTSGRCh37
Build 366132,662,563 - 132,662,787RGDNCBI36
Celera6133,367,751 - 133,367,975RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,195,996 - 130,196,220UniSTS
REN30919  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,621,066 - 132,621,321UniSTSGRCh37
Build 366132,662,759 - 132,663,014RGDNCBI36
Celera6133,367,947 - 133,368,202RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,196,192 - 130,196,447UniSTS
REN30920  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,621,299 - 132,621,525UniSTSGRCh37
Build 366132,662,992 - 132,663,218RGDNCBI36
Celera6133,368,180 - 133,368,406RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,196,425 - 130,196,651UniSTS
REN30921  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,621,508 - 132,621,761UniSTSGRCh37
Build 366132,663,201 - 132,663,454RGDNCBI36
Celera6133,368,389 - 133,368,642RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,196,634 - 130,196,887UniSTS
REN30922  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,621,715 - 132,621,964UniSTSGRCh37
Build 366132,663,408 - 132,663,657RGDNCBI36
Celera6133,368,596 - 133,368,845RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,196,841 - 130,197,090UniSTS
REN30923  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,621,941 - 132,622,206UniSTSGRCh37
Build 366132,663,634 - 132,663,899RGDNCBI36
Celera6133,368,822 - 133,369,087RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,197,067 - 130,197,332UniSTS
REN30924  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,622,106 - 132,622,334UniSTSGRCh37
Build 366132,663,799 - 132,664,027RGDNCBI36
Celera6133,368,987 - 133,369,215RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,197,232 - 130,197,460UniSTS
REN30925  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,622,304 - 132,622,567UniSTSGRCh37
Build 366132,663,997 - 132,664,260RGDNCBI36
Celera6133,369,185 - 133,369,448RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,197,430 - 130,197,691UniSTS
REN30926  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,622,548 - 132,622,777UniSTSGRCh37
Build 366132,664,241 - 132,664,470RGDNCBI36
Celera6133,369,429 - 133,369,658RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,197,672 - 130,197,901UniSTS
REN30927  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,622,754 - 132,623,004UniSTSGRCh37
Build 366132,664,447 - 132,664,697RGDNCBI36
Celera6133,369,635 - 133,369,885RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,197,878 - 130,198,128UniSTS
REN30928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,622,981 - 132,623,238UniSTSGRCh37
Build 366132,664,674 - 132,664,931RGDNCBI36
Celera6133,369,862 - 133,370,119RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,198,105 - 130,198,362UniSTS
REN30929  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,623,171 - 132,623,425UniSTSGRCh37
Build 366132,664,864 - 132,665,118RGDNCBI36
Celera6133,370,052 - 133,370,306RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,198,295 - 130,198,549UniSTS
REN30930  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,623,395 - 132,623,657UniSTSGRCh37
Build 366132,665,088 - 132,665,350RGDNCBI36
Celera6133,370,276 - 133,370,539RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,198,519 - 130,198,781UniSTS
REN30931  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,623,570 - 132,623,813UniSTSGRCh37
Build 366132,665,263 - 132,665,506RGDNCBI36
Celera6133,370,451 - 133,370,695RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,198,694 - 130,198,937UniSTS
REN30932  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,623,791 - 132,624,040UniSTSGRCh37
Build 366132,665,484 - 132,665,733RGDNCBI36
Celera6133,370,673 - 133,370,922RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,198,915 - 130,199,164UniSTS
REN30933  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,624,038 - 132,624,269UniSTSGRCh37
Build 366132,665,731 - 132,665,962RGDNCBI36
Celera6133,370,920 - 133,371,151RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,199,162 - 130,199,393UniSTS
REN30934  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,624,246 - 132,624,482UniSTSGRCh37
Build 366132,665,939 - 132,666,175RGDNCBI36
Celera6133,371,128 - 133,371,364RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,199,370 - 130,199,606UniSTS
REN30935  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,624,455 - 132,624,717UniSTSGRCh37
Build 366132,666,148 - 132,666,410RGDNCBI36
Celera6133,371,337 - 133,371,599RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,199,579 - 130,199,841UniSTS
REN30936  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,624,605 - 132,624,846UniSTSGRCh37
Build 366132,666,298 - 132,666,539RGDNCBI36
Celera6133,371,487 - 133,371,728RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,199,729 - 130,199,970UniSTS
REN30937  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,624,798 - 132,625,055UniSTSGRCh37
Build 366132,666,491 - 132,666,748RGDNCBI36
Celera6133,371,680 - 133,371,937RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,199,922 - 130,200,149UniSTS
REN30938  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,625,027 - 132,625,271UniSTSGRCh37
Build 366132,666,720 - 132,666,964RGDNCBI36
Celera6133,371,909 - 133,372,153RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,200,121 - 130,200,365UniSTS
REN30939  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,625,225 - 132,625,469UniSTSGRCh37
Build 366132,666,918 - 132,667,162RGDNCBI36
Celera6133,372,107 - 133,372,351RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,200,319 - 130,200,563UniSTS
REN30940  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,625,460 - 132,625,707UniSTSGRCh37
Build 366132,667,153 - 132,667,400RGDNCBI36
Celera6133,372,342 - 133,372,589RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,200,554 - 130,200,801UniSTS
REN30941  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,625,684 - 132,625,927UniSTSGRCh37
Build 366132,667,377 - 132,667,620RGDNCBI36
Celera6133,372,566 - 133,372,809RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,200,778 - 130,201,021UniSTS
REN30942  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,625,925 - 132,626,150UniSTSGRCh37
Build 366132,667,618 - 132,667,843RGDNCBI36
Celera6133,372,807 - 133,373,032RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,201,019 - 130,201,244UniSTS
REN30943  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,626,104 - 132,626,354UniSTSGRCh37
Build 366132,667,797 - 132,668,047RGDNCBI36
Celera6133,372,986 - 133,373,236RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,201,198 - 130,201,448UniSTS
REN30944  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,626,332 - 132,626,581UniSTSGRCh37
GRCh372231,355,974 - 231,356,220UniSTSGRCh37
Build 362231,064,218 - 231,064,464RGDNCBI36
Celera6133,373,214 - 133,373,463UniSTS
Celera2225,132,150 - 225,132,396RGD
Cytogenetic Map6q23.2UniSTS
Cytogenetic Map2q37.1UniSTS
HuRef6130,201,426 - 130,201,675UniSTS
HuRef5125,450,621 - 125,450,869UniSTS
REN30946  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,626,808 - 132,627,033UniSTSGRCh37
Build 366132,668,501 - 132,668,726RGDNCBI36
Celera6133,373,690 - 133,373,915RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,201,902 - 130,202,127UniSTS
REN30947  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,627,009 - 132,627,274UniSTSGRCh37
Build 366132,668,702 - 132,668,967RGDNCBI36
Celera6133,373,891 - 133,374,156RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,202,103 - 130,202,368UniSTS
REN30948  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,627,129 - 132,627,353UniSTSGRCh37
Build 366132,668,822 - 132,669,046RGDNCBI36
Celera6133,374,011 - 133,374,235RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,202,223 - 130,202,447UniSTS
REN30949  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,627,297 - 132,627,545UniSTSGRCh37
Build 366132,668,990 - 132,669,238RGDNCBI36
Celera6133,374,179 - 133,374,427RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,202,391 - 130,202,639UniSTS
REN30951  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,627,711 - 132,627,971UniSTSGRCh37
Build 366132,669,404 - 132,669,664RGDNCBI36
Celera6133,374,593 - 133,374,853RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,202,805 - 130,203,065UniSTS
REN30952  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,628,086 - 132,628,331UniSTSGRCh37
Build 366132,669,779 - 132,670,024RGDNCBI36
Celera6133,374,968 - 133,375,213RGD
Cytogenetic Map6q23.2UniSTS
HuRef1392,246,811 - 92,247,051UniSTS
HuRef6130,203,180 - 130,203,425UniSTS
REN30953  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,628,128 - 132,628,390UniSTSGRCh37
Build 366132,669,821 - 132,670,083RGDNCBI36
Celera6133,375,010 - 133,375,272RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,203,222 - 130,203,484UniSTS
REN30954  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,628,364 - 132,628,594UniSTSGRCh37
Build 366132,670,057 - 132,670,287RGDNCBI36
Celera6133,375,246 - 133,375,476RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,203,458 - 130,203,688UniSTS
REN30955  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,628,666 - 132,628,897UniSTSGRCh37
Build 366132,670,359 - 132,670,590RGDNCBI36
Celera6133,375,548 - 133,375,779RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,203,760 - 130,203,991UniSTS
REN30956  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,628,875 - 132,629,124UniSTSGRCh37
Build 366132,670,568 - 132,670,817RGDNCBI36
Celera6133,375,757 - 133,376,006RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,203,969 - 130,204,218UniSTS
REN30957  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,629,100 - 132,629,339UniSTSGRCh37
Build 366132,670,793 - 132,671,032RGDNCBI36
Celera6133,375,982 - 133,376,221RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,204,194 - 130,204,433UniSTS
REN30958  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,629,316 - 132,629,552UniSTSGRCh37
Build 366132,671,009 - 132,671,245RGDNCBI36
Celera6133,376,198 - 133,376,434RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,204,410 - 130,204,646UniSTS
REN30959  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,630,021 - 132,630,289UniSTSGRCh37
Build 366132,671,714 - 132,671,982RGDNCBI36
Celera6133,376,903 - 133,377,171RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,205,115 - 130,205,383UniSTS
REN30960  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,630,266 - 132,630,505UniSTSGRCh37
Build 366132,671,959 - 132,672,198RGDNCBI36
Celera6133,377,148 - 133,377,387RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,205,360 - 130,205,599UniSTS
REN30961  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,630,472 - 132,630,716UniSTSGRCh37
Build 366132,672,165 - 132,672,409RGDNCBI36
Celera6133,377,354 - 133,377,598RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,205,566 - 130,205,810UniSTS
REN30962  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,630,673 - 132,630,929UniSTSGRCh37
Build 366132,672,366 - 132,672,622RGDNCBI36
Celera6133,377,555 - 133,377,811RGD
Cytogenetic Map6q23.2UniSTS
HuRefX106,293,914 - 106,294,189UniSTS
HuRef6130,205,767 - 130,206,023UniSTS
REN30963  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,630,806 - 132,631,039UniSTSGRCh37
Build 366132,672,499 - 132,672,732RGDNCBI36
Celera6133,377,688 - 133,377,921RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,205,900 - 130,206,133UniSTS
REN30964  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,630,971 - 132,631,218UniSTSGRCh37
Build 366132,672,664 - 132,672,911RGDNCBI36
Celera6133,377,853 - 133,378,100RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,206,065 - 130,206,312UniSTS
REN30965  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,631,603 - 132,631,867UniSTSGRCh37
Build 366132,673,296 - 132,673,560RGDNCBI36
Celera6133,378,485 - 133,378,749RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,206,697 - 130,206,961UniSTS
REN30966  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,631,783 - 132,632,034UniSTSGRCh37
Build 366132,673,476 - 132,673,727RGDNCBI36
Celera6133,378,665 - 133,378,916RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,206,877 - 130,207,128UniSTS
REN30967  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,632,010 - 132,632,279UniSTSGRCh37
Build 366132,673,703 - 132,673,972RGDNCBI36
Celera6133,378,892 - 133,379,161RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,207,104 - 130,207,373UniSTS
REN30968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,632,252 - 132,632,501UniSTSGRCh37
Build 366132,673,945 - 132,674,194RGDNCBI36
Celera6133,379,134 - 133,379,383RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,207,346 - 130,207,595UniSTS
REN30969  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,632,476 - 132,632,718UniSTSGRCh37
Build 366132,674,169 - 132,674,411RGDNCBI36
Celera6133,379,358 - 133,379,600RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,207,570 - 130,207,812UniSTS
REN30970  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,632,695 - 132,632,949UniSTSGRCh37
Build 366132,674,388 - 132,674,642RGDNCBI36
Celera6133,379,577 - 133,379,831RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,207,789 - 130,208,043UniSTS
REN30971  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,632,936 - 132,633,171UniSTSGRCh37
Build 366132,674,629 - 132,674,864RGDNCBI36
Celera6133,379,818 - 133,380,053RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,208,030 - 130,208,265UniSTS
REN30972  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,633,116 - 132,633,352UniSTSGRCh37
Build 366132,674,809 - 132,675,045RGDNCBI36
Celera6133,379,998 - 133,380,234RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,208,210 - 130,208,446UniSTS
REN30973  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,633,312 - 132,633,576UniSTSGRCh37
Build 366132,675,005 - 132,675,269RGDNCBI36
Celera6133,380,194 - 133,380,458RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,208,406 - 130,208,670UniSTS
REN30974  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,633,566 - 132,633,801UniSTSGRCh37
Build 366132,675,259 - 132,675,494RGDNCBI36
Celera6133,380,448 - 133,380,683RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,208,660 - 130,208,895UniSTS
REN30975  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,633,768 - 132,634,004UniSTSGRCh37
Build 366132,675,461 - 132,675,697RGDNCBI36
Celera6133,380,650 - 133,380,886RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,208,862 - 130,209,098UniSTS
REN30976  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,633,971 - 132,634,197UniSTSGRCh37
Build 366132,675,664 - 132,675,890RGDNCBI36
Celera6133,380,853 - 133,381,079RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,209,065 - 130,209,291UniSTS
REN30977  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,634,171 - 132,634,426UniSTSGRCh37
Build 366132,675,864 - 132,676,119RGDNCBI36
Celera6133,381,053 - 133,381,308RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,209,265 - 130,209,520UniSTS
REN30978  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,634,391 - 132,634,634UniSTSGRCh37
Build 366132,676,084 - 132,676,327RGDNCBI36
Celera6133,381,273 - 133,381,516RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,209,485 - 130,209,728UniSTS
REN30979  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,634,541 - 132,634,781UniSTSGRCh37
Build 366132,676,234 - 132,676,474RGDNCBI36
Celera6133,381,423 - 133,381,663RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,209,635 - 130,209,875UniSTS
REN30980  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,635,107 - 132,635,331UniSTSGRCh37
Build 366132,676,800 - 132,677,024RGDNCBI36
Celera6133,381,989 - 133,382,213RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,210,201 - 130,210,425UniSTS
REN30981  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,635,314 - 132,635,559UniSTSGRCh37
Build 366132,677,007 - 132,677,252RGDNCBI36
Celera6133,382,196 - 133,382,441RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,210,408 - 130,210,653UniSTS
REN30982  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,635,536 - 132,635,783UniSTSGRCh37
Build 366132,677,229 - 132,677,476RGDNCBI36
Celera6133,382,418 - 133,382,665RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,210,630 - 130,210,877UniSTS
REN30983  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,635,756 - 132,636,006UniSTSGRCh37
Build 366132,677,449 - 132,677,699RGDNCBI36
Celera6133,382,638 - 133,382,888RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,210,850 - 130,211,100UniSTS
REN30984  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,635,974 - 132,636,223UniSTSGRCh37
Build 366132,677,667 - 132,677,916RGDNCBI36
Celera6133,382,856 - 133,383,105RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,211,068 - 130,211,317UniSTS
REN30985  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,636,197 - 132,636,428UniSTSGRCh37
Build 366132,677,890 - 132,678,121RGDNCBI36
Celera6133,383,079 - 133,383,310RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,211,291 - 130,211,522UniSTS
REN30986  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,636,405 - 132,636,649UniSTSGRCh37
Build 366132,678,098 - 132,678,342RGDNCBI36
Celera6133,383,287 - 133,383,531RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,211,499 - 130,211,743UniSTS
REN30987  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,636,633 - 132,636,865UniSTSGRCh37
Build 366132,678,326 - 132,678,558RGDNCBI36
Celera6133,383,515 - 133,383,747RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,211,727 - 130,211,959UniSTS
REN30988  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,636,788 - 132,637,020UniSTSGRCh37
Build 366132,678,481 - 132,678,713RGDNCBI36
Celera6133,383,670 - 133,383,902RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,211,882 - 130,212,114UniSTS
REN30989  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,636,983 - 132,637,219UniSTSGRCh37
Build 366132,678,676 - 132,678,912RGDNCBI36
Celera6133,383,865 - 133,384,101RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,212,077 - 130,212,313UniSTS
REN30990  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,637,208 - 132,637,477UniSTSGRCh37
Build 366132,678,901 - 132,679,170RGDNCBI36
Celera6133,384,090 - 133,384,360RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,212,302 - 130,212,571UniSTS
REN30991  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,637,448 - 132,637,698UniSTSGRCh37
Build 366132,679,141 - 132,679,391RGDNCBI36
Celera6133,384,331 - 133,384,581RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,212,542 - 130,212,792UniSTS
REN30992  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,637,673 - 132,637,902UniSTSGRCh37
Build 366132,679,366 - 132,679,595RGDNCBI36
Celera6133,384,556 - 133,384,785RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,212,767 - 130,212,996UniSTS
REN30993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,637,877 - 132,638,127UniSTSGRCh37
Build 366132,679,570 - 132,679,820RGDNCBI36
Celera6133,384,760 - 133,385,010RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,212,971 - 130,213,221UniSTS
REN30994  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,638,123 - 132,638,358UniSTSGRCh37
Build 366132,679,816 - 132,680,051RGDNCBI36
Celera6133,385,006 - 133,385,241RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,213,217 - 130,213,452UniSTS
REN30995  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,638,333 - 132,638,591UniSTSGRCh37
Build 366132,680,026 - 132,680,284RGDNCBI36
Celera6133,385,216 - 133,385,474RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,213,427 - 130,213,685UniSTS
REN30996  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,638,565 - 132,638,805UniSTSGRCh37
Build 366132,680,258 - 132,680,498RGDNCBI36
Celera6133,385,448 - 133,385,688RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,213,659 - 130,213,899UniSTS
REN30997  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,638,751 - 132,638,975UniSTSGRCh37
Build 366132,680,444 - 132,680,668RGDNCBI36
Celera6133,385,634 - 133,385,858RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,213,845 - 130,214,069UniSTS
REN30998  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,638,936 - 132,639,186UniSTSGRCh37
Build 366132,680,629 - 132,680,879RGDNCBI36
Celera6133,385,819 - 133,386,069RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,214,030 - 130,214,280UniSTS
REN30999  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,639,163 - 132,639,431UniSTSGRCh37
Build 366132,680,856 - 132,681,124RGDNCBI36
Celera6133,386,046 - 133,386,314RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,214,257 - 130,214,525UniSTS
REN31000  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,639,427 - 132,639,683UniSTSGRCh37
Build 366132,681,120 - 132,681,376RGDNCBI36
Celera6133,386,310 - 133,386,566RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,214,521 - 130,214,777UniSTS
REN31001  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,639,657 - 132,639,929UniSTSGRCh37
Build 366132,681,350 - 132,681,622RGDNCBI36
Celera6133,386,540 - 133,386,812RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,214,751 - 130,215,023UniSTS
REN31002  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,639,833 - 132,640,101UniSTSGRCh37
Build 366132,681,526 - 132,681,794RGDNCBI36
Celera6133,386,716 - 133,386,984RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,214,927 - 130,215,195UniSTS
REN31003  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,640,089 - 132,640,327UniSTSGRCh37
Build 366132,681,782 - 132,682,020RGDNCBI36
Celera6133,386,972 - 133,387,210RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,215,183 - 130,215,421UniSTS
REN31004  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,640,311 - 132,640,569UniSTSGRCh37
Build 366132,682,004 - 132,682,262RGDNCBI36
Celera6133,387,194 - 133,387,452RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,215,405 - 130,215,663UniSTS
REN31005  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,640,548 - 132,640,785UniSTSGRCh37
Build 366132,682,241 - 132,682,478RGDNCBI36
Celera6133,387,431 - 133,387,668RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,215,642 - 130,215,879UniSTS
REN31006  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,640,754 - 132,641,000UniSTSGRCh37
Build 366132,682,447 - 132,682,693RGDNCBI36
Celera6133,387,637 - 133,387,883RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,215,848 - 130,216,094UniSTS
REN31007  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,640,991 - 132,641,218UniSTSGRCh37
Build 366132,682,684 - 132,682,911RGDNCBI36
Celera6133,387,874 - 133,388,101RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,216,085 - 130,216,312UniSTS
REN31008  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,641,195 - 132,641,460UniSTSGRCh37
Build 366132,682,888 - 132,683,153RGDNCBI36
Celera6133,388,078 - 133,388,343RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,216,289 - 130,216,554UniSTS
REN31009  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,641,437 - 132,641,688UniSTSGRCh37
Build 366132,683,130 - 132,683,381RGDNCBI36
Celera6133,388,320 - 133,388,571RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,216,531 - 130,216,782UniSTS
REN31010  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,641,665 - 132,641,893UniSTSGRCh37
Build 366132,683,358 - 132,683,586RGDNCBI36
Celera6133,388,548 - 133,388,776RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,216,759 - 130,216,987UniSTS
REN31011  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,641,838 - 132,642,088UniSTSGRCh37
Build 366132,683,531 - 132,683,781RGDNCBI36
Celera6133,388,721 - 133,388,971RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,216,932 - 130,217,182UniSTS
REN31012  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,642,036 - 132,642,301UniSTSGRCh37
Build 366132,683,729 - 132,683,994RGDNCBI36
Celera6133,388,919 - 133,389,184RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,217,130 - 130,217,395UniSTS
REN31013  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,642,278 - 132,642,540UniSTSGRCh37
Build 366132,683,971 - 132,684,233RGDNCBI36
Celera6133,389,161 - 133,389,423RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,217,372 - 130,217,634UniSTS
REN31014  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,642,513 - 132,642,765UniSTSGRCh37
Build 366132,684,206 - 132,684,458RGDNCBI36
Celera6133,389,396 - 133,389,648RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,217,607 - 130,217,859UniSTS
REN31015  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,642,747 - 132,642,971UniSTSGRCh37
Build 366132,684,440 - 132,684,664RGDNCBI36
Celera6133,389,630 - 133,389,854RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,217,841 - 130,218,065UniSTS
REN31016  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,642,940 - 132,643,189UniSTSGRCh37
Build 366132,684,633 - 132,684,882RGDNCBI36
Celera6133,389,823 - 133,390,072RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,218,034 - 130,218,283UniSTS
REN31017  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,643,161 - 132,643,409UniSTSGRCh37
Build 366132,684,854 - 132,685,102RGDNCBI36
Celera6133,390,044 - 133,390,292RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,218,255 - 130,218,503UniSTS
REN31018  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,643,331 - 132,643,566UniSTSGRCh37
Build 366132,685,024 - 132,685,259RGDNCBI36
Celera6133,390,214 - 133,390,449RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,218,425 - 130,218,660UniSTS
REN31019  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,643,540 - 132,643,768UniSTSGRCh37
Build 366132,685,233 - 132,685,461RGDNCBI36
Celera6133,390,423 - 133,390,651RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,218,634 - 130,218,862UniSTS
REN31020  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,643,757 - 132,643,989UniSTSGRCh37
Build 366132,685,450 - 132,685,682RGDNCBI36
Celera6133,390,640 - 133,390,872RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,218,851 - 130,219,083UniSTS
REN31021  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,643,966 - 132,644,220UniSTSGRCh37
Build 366132,685,659 - 132,685,913RGDNCBI36
Celera6133,390,849 - 133,391,103RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,219,060 - 130,219,314UniSTS
REN31022  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,644,197 - 132,644,443UniSTSGRCh37
Build 366132,685,890 - 132,686,136RGDNCBI36
Celera6133,391,080 - 133,391,326RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,219,291 - 130,219,537UniSTS
REN31023  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,644,442 - 132,644,694UniSTSGRCh37
Build 366132,686,135 - 132,686,387RGDNCBI36
Celera6133,391,325 - 133,391,577RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,219,536 - 130,219,788UniSTS
REN31024  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,644,682 - 132,644,942UniSTSGRCh37
Build 366132,686,375 - 132,686,635RGDNCBI36
Celera6133,391,565 - 133,391,825RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,219,776 - 130,220,036UniSTS
REN31025  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,644,935 - 132,645,185UniSTSGRCh37
Build 366132,686,628 - 132,686,878RGDNCBI36
Celera6133,391,818 - 133,392,068RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,220,029 - 130,220,279UniSTS
REN31026  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,645,169 - 132,645,413UniSTSGRCh37
Build 366132,686,862 - 132,687,106RGDNCBI36
Celera6133,392,052 - 133,392,296RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,220,263 - 130,220,507UniSTS
REN31027  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,645,390 - 132,645,640UniSTSGRCh37
Build 366132,687,083 - 132,687,333RGDNCBI36
Celera6133,392,273 - 133,392,523RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,220,484 - 130,220,734UniSTS
REN31028  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,645,615 - 132,645,863UniSTSGRCh37
Build 366132,687,308 - 132,687,556RGDNCBI36
Celera6133,392,498 - 133,392,746RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,220,709 - 130,220,957UniSTS
REN31029  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,645,861 - 132,646,106UniSTSGRCh37
Build 366132,687,554 - 132,687,799RGDNCBI36
Celera6133,392,744 - 133,392,989RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,220,955 - 130,221,200UniSTS
REN31030  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,067 - 132,646,292UniSTSGRCh37
Build 366132,687,760 - 132,687,985RGDNCBI36
Celera6133,392,950 - 133,393,177RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,221,161 - 130,221,388UniSTS
REN31031  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,252 - 132,646,521UniSTSGRCh37
Build 366132,687,945 - 132,688,214RGDNCBI36
Celera6133,393,137 - 133,393,406RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,221,348 - 130,221,617UniSTS
REN31032  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,519 - 132,646,743UniSTSGRCh37
Build 366132,688,212 - 132,688,436RGDNCBI36
Celera6133,393,404 - 133,393,628RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,221,615 - 130,221,839UniSTS
REN31033  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,709 - 132,646,960UniSTSGRCh37
Build 366132,688,402 - 132,688,653RGDNCBI36
Celera6133,393,594 - 133,393,845RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,221,805 - 130,222,056UniSTS
REN31034  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,948 - 132,647,197UniSTSGRCh37
Build 366132,688,641 - 132,688,890RGDNCBI36
Celera6133,393,833 - 133,394,082RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,222,044 - 130,222,293UniSTS
REN31035  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,647,050 - 132,647,274UniSTSGRCh37
Build 366132,688,743 - 132,688,967RGDNCBI36
Celera6133,393,935 - 133,394,159RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,222,146 - 130,222,370UniSTS
REN31036  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,647,247 - 132,647,471UniSTSGRCh37
Build 366132,688,940 - 132,689,164RGDNCBI36
Celera6133,394,132 - 133,394,356RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,222,343 - 130,222,567UniSTS
REN31037  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,647,516 - 132,647,770UniSTSGRCh37
Build 366132,689,209 - 132,689,463RGDNCBI36
Celera6133,394,401 - 133,394,655RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,222,612 - 130,222,866UniSTS
REN31038  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,647,756 - 132,647,980UniSTSGRCh37
Build 366132,689,449 - 132,689,673RGDNCBI36
Celera6133,394,641 - 133,394,865RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,222,852 - 130,223,076UniSTS
REN31039  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,647,949 - 132,648,194UniSTSGRCh37
Build 366132,689,642 - 132,689,887RGDNCBI36
Celera6133,394,834 - 133,395,079RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,223,045 - 130,223,290UniSTS
REN31040  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,648,145 - 132,648,391UniSTSGRCh37
Build 366132,689,838 - 132,690,084RGDNCBI36
Celera6133,395,030 - 133,395,276RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,223,241 - 130,223,487UniSTS
REN31041  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,648,365 - 132,648,597UniSTSGRCh37
Build 366132,690,058 - 132,690,290RGDNCBI36
Celera6133,395,250 - 133,395,482RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,223,461 - 130,223,693UniSTS
REN31042  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,648,571 - 132,648,840UniSTSGRCh37
Build 366132,690,264 - 132,690,533RGDNCBI36
Celera6133,395,456 - 133,395,725RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,223,667 - 130,223,936UniSTS
REN31043  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,648,837 - 132,649,079UniSTSGRCh37
Build 366132,690,530 - 132,690,772RGDNCBI36
Celera6133,395,722 - 133,395,964RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,223,933 - 130,224,175UniSTS
REN31044  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,649,055 - 132,649,314UniSTSGRCh37
Build 366132,690,748 - 132,691,007RGDNCBI36
Celera6133,395,940 - 133,396,199RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,224,151 - 130,224,410UniSTS
REN31045  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,649,294 - 132,649,554UniSTSGRCh37
Build 366132,690,987 - 132,691,247RGDNCBI36
Celera6133,396,179 - 133,396,439RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,224,390 - 130,224,650UniSTS
REN31046  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,649,535 - 132,649,791UniSTSGRCh37
Build 366132,691,228 - 132,691,484RGDNCBI36
Celera6133,396,420 - 133,396,676RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,224,631 - 130,224,887UniSTS
REN31047  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,649,790 - 132,650,047UniSTSGRCh37
Build 366132,691,483 - 132,691,740RGDNCBI36
Celera6133,396,675 - 133,396,932RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,224,886 - 130,225,143UniSTS
REN31048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,649,877 - 132,650,101UniSTSGRCh37
Build 366132,691,570 - 132,691,794RGDNCBI36
Celera6133,396,762 - 133,396,986RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,224,973 - 130,225,197UniSTS
REN31049  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,650,417 - 132,650,660UniSTSGRCh37
Build 366132,692,110 - 132,692,353RGDNCBI36
Celera6133,397,302 - 133,397,545RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,225,513 - 130,225,756UniSTS
REN31050  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,650,647 - 132,650,902UniSTSGRCh37
Build 366132,692,340 - 132,692,595RGDNCBI36
Celera6133,397,532 - 133,397,787RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,225,743 - 130,225,998UniSTS
REN31051  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,650,886 - 132,651,145UniSTSGRCh37
Build 366132,692,579 - 132,692,838RGDNCBI36
Celera6133,397,771 - 133,398,030RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,225,982 - 130,226,241UniSTS
REN31052  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,651,079 - 132,651,303UniSTSGRCh37
Build 366132,692,772 - 132,692,996RGDNCBI36
Celera6133,397,964 - 133,398,188RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,226,175 - 130,226,399UniSTS
REN31053  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,651,279 - 132,651,525UniSTSGRCh37
Build 366132,692,972 - 132,693,218RGDNCBI36
Celera6133,398,164 - 133,398,410RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,226,375 - 130,226,621UniSTS
REN31054  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,651,516 - 132,651,751UniSTSGRCh37
Build 366132,693,209 - 132,693,444RGDNCBI36
Celera6133,398,401 - 133,398,636RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,226,612 - 130,226,847UniSTS
REN31055  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,651,745 - 132,651,995UniSTSGRCh37
Build 366132,693,438 - 132,693,688RGDNCBI36
Celera6133,398,630 - 133,398,880RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,226,841 - 130,227,091UniSTS
REN31056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,651,972 - 132,652,222UniSTSGRCh37
Build 366132,693,665 - 132,693,915RGDNCBI36
Celera6133,398,857 - 133,399,107RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,227,068 - 130,227,318UniSTS
REN31057  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,652,183 - 132,652,430UniSTSGRCh37
Build 366132,693,876 - 132,694,123RGDNCBI36
Celera6133,399,068 - 133,399,315RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,227,279 - 130,227,526UniSTS
REN31058  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,652,407 - 132,652,681UniSTSGRCh37
Build 366132,694,100 - 132,694,374RGDNCBI36
Celera6133,399,292 - 133,399,566RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,227,503 - 130,227,777UniSTS
REN31059  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,652,674 - 132,652,930UniSTSGRCh37
Build 366132,694,367 - 132,694,623RGDNCBI36
Celera6133,399,559 - 133,399,815RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,227,770 - 130,228,026UniSTS
REN31060  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,652,918 - 132,653,178UniSTSGRCh37
Build 366132,694,611 - 132,694,871RGDNCBI36
Celera6133,399,803 - 133,400,063RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,228,014 - 130,228,274UniSTS
REN31061  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,653,150 - 132,653,419UniSTSGRCh37
Build 366132,694,843 - 132,695,112RGDNCBI36
Celera6133,400,035 - 133,400,304RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,228,246 - 130,228,515UniSTS
REN31062  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,653,397 - 132,653,633UniSTSGRCh37
Build 366132,695,090 - 132,695,326RGDNCBI36
Celera6133,400,282 - 133,400,518RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,228,493 - 130,228,729UniSTS
REN31063  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,653,605 - 132,653,835UniSTSGRCh37
Build 366132,695,298 - 132,695,528RGDNCBI36
Celera6133,400,490 - 133,400,720RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,228,701 - 130,228,931UniSTS
REN31064  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,653,812 - 132,654,061UniSTSGRCh37
Build 366132,695,505 - 132,695,754RGDNCBI36
Celera6133,400,697 - 133,400,946RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,228,908 - 130,229,157UniSTS
REN31065  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,653,928 - 132,654,198UniSTSGRCh37
Build 366132,695,621 - 132,695,891RGDNCBI36
Celera6133,400,813 - 133,401,083RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,229,024 - 130,229,294UniSTS
REN31066  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,654,499 - 132,654,740UniSTSGRCh37
Build 366132,696,192 - 132,696,433RGDNCBI36
Celera6133,401,384 - 133,401,625RGD
Cytogenetic Map6q23.2UniSTS
REN31067  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,654,733 - 132,654,999UniSTSGRCh37
Build 366132,696,426 - 132,696,692RGDNCBI36
Celera6133,401,618 - 133,401,884RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,229,839 - 130,230,105UniSTS
REN31068  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,654,998 - 132,655,250UniSTSGRCh37
Build 366132,696,691 - 132,696,943RGDNCBI36
Celera6133,401,883 - 133,402,135RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,230,104 - 130,230,356UniSTS
REN31069  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,655,244 - 132,655,498UniSTSGRCh37
Build 366132,696,937 - 132,697,191RGDNCBI36
Celera6133,402,129 - 133,402,383RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,230,350 - 130,230,604UniSTS
REN31070  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,655,492 - 132,655,740UniSTSGRCh37
Build 366132,697,185 - 132,697,433RGDNCBI36
Celera6133,402,377 - 133,402,625RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,230,598 - 130,230,846UniSTS
REN31071  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,655,728 - 132,655,979UniSTSGRCh37
Build 366132,697,421 - 132,697,672RGDNCBI36
Celera6133,402,613 - 133,402,864RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,230,834 - 130,231,085UniSTS
REN31072  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,655,939 - 132,656,186UniSTSGRCh37
Build 366132,697,632 - 132,697,879RGDNCBI36
Celera6133,402,824 - 133,403,071RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,231,045 - 130,231,292UniSTS
REN31073  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,656,179 - 132,656,422UniSTSGRCh37
Build 366132,697,872 - 132,698,115RGDNCBI36
Celera6133,403,064 - 133,403,307RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,231,285 - 130,231,528UniSTS
REN31074  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,656,393 - 132,656,654UniSTSGRCh37
Build 366132,698,086 - 132,698,347RGDNCBI36
Celera6133,403,278 - 133,403,539RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,231,499 - 130,231,760UniSTS
REN31075  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,656,634 - 132,656,859UniSTSGRCh37
Build 366132,698,327 - 132,698,552RGDNCBI36
Celera6133,403,519 - 133,403,744RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,231,740 - 130,231,965UniSTS
REN31076  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,656,854 - 132,657,104UniSTSGRCh37
Build 366132,698,547 - 132,698,797RGDNCBI36
Celera6133,403,739 - 133,403,989RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,231,960 - 130,232,210UniSTS
REN31077  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,657,080 - 132,657,340UniSTSGRCh37
Build 366132,698,773 - 132,699,033RGDNCBI36
Celera6133,403,965 - 133,404,225RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,232,186 - 130,232,446UniSTS
REN31078  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,657,317 - 132,657,543UniSTSGRCh37
Build 366132,699,010 - 132,699,236RGDNCBI36
Celera6133,404,202 - 133,404,428RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,232,423 - 130,232,649UniSTS
REN31079  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,657,511 - 132,657,760UniSTSGRCh37
Build 366132,699,204 - 132,699,453RGDNCBI36
Celera6133,404,396 - 133,404,645RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,232,617 - 130,232,866UniSTS
REN31080  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,657,737 - 132,657,992UniSTSGRCh37
Build 366132,699,430 - 132,699,685RGDNCBI36
Celera6133,404,622 - 133,404,877RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,232,843 - 130,233,098UniSTS
REN31081  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,657,969 - 132,658,224UniSTSGRCh37
Build 366132,699,662 - 132,699,917RGDNCBI36
Celera6133,404,854 - 133,405,109RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,233,075 - 130,233,330UniSTS
REN31082  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,658,204 - 132,658,458UniSTSGRCh37
Build 366132,699,897 - 132,700,151RGDNCBI36
Celera6133,405,089 - 133,405,343RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,233,310 - 130,233,564UniSTS
REN31083  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,658,443 - 132,658,680UniSTSGRCh37
Build 366132,700,136 - 132,700,373RGDNCBI36
Celera6133,405,328 - 133,405,565RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,233,549 - 130,233,786UniSTS
REN31084  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,658,568 - 132,658,792UniSTSGRCh37
Build 366132,700,261 - 132,700,485RGDNCBI36
Celera6133,405,453 - 133,405,677RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,233,674 - 130,233,898UniSTS
REN31085  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,658,785 - 132,659,032UniSTSGRCh37
Build 366132,700,478 - 132,700,725RGDNCBI36
Celera6133,405,670 - 133,405,917RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,233,891 - 130,234,138UniSTS
REN31086  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,659,006 - 132,659,242UniSTSGRCh37
Build 366132,700,699 - 132,700,935RGDNCBI36
Celera6133,405,891 - 133,406,127RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,234,112 - 130,234,348UniSTS
REN31087  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,659,219 - 132,659,452UniSTSGRCh37
Build 366132,700,912 - 132,701,145RGDNCBI36
Celera6133,406,104 - 133,406,337RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,234,325 - 130,234,558UniSTS
REN31088  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,659,425 - 132,659,686UniSTSGRCh37
Build 366132,701,118 - 132,701,379RGDNCBI36
Celera6133,406,310 - 133,406,571RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,234,531 - 130,234,792UniSTS
REN31089  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,659,678 - 132,659,931UniSTSGRCh37
Build 366132,701,371 - 132,701,624RGDNCBI36
Celera6133,406,563 - 133,406,816RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,234,784 - 130,235,037UniSTS
REN31090  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,659,908 - 132,660,154UniSTSGRCh37
Build 366132,701,601 - 132,701,847RGDNCBI36
Celera6133,406,793 - 133,407,039RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,235,014 - 130,235,260UniSTS
REN31091  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,660,123 - 132,660,376UniSTSGRCh37
Build 366132,701,816 - 132,702,069RGDNCBI36
Celera6133,407,008 - 133,407,261RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,235,229 - 130,235,482UniSTS
REN31092  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,660,353 - 132,660,613UniSTSGRCh37
Build 366132,702,046 - 132,702,306RGDNCBI36
Celera6133,407,238 - 133,407,498RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,235,459 - 130,235,719UniSTS
REN31093  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,660,589 - 132,660,829UniSTSGRCh37
Build 366132,702,282 - 132,702,522RGDNCBI36
Celera6133,407,474 - 133,407,714RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,235,695 - 130,235,935UniSTS
REN31094  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,660,809 - 132,661,046UniSTSGRCh37
Build 366132,702,502 - 132,702,739RGDNCBI36
Celera6133,407,694 - 133,407,931RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,235,915 - 130,236,152UniSTS
REN31095  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,660,879 - 132,661,133UniSTSGRCh37
Build 366132,702,572 - 132,702,826RGDNCBI36
Celera6133,407,764 - 133,408,018RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,235,985 - 130,236,239UniSTS
REN31096  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,661,109 - 132,661,379UniSTSGRCh37
Build 366132,702,802 - 132,703,072RGDNCBI36
Celera6133,407,994 - 133,408,264RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,236,215 - 130,236,485UniSTS
REN31097  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,661,346 - 132,661,579UniSTSGRCh37
Build 366132,703,039 - 132,703,272RGDNCBI36
Celera6133,408,231 - 133,408,464RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,236,452 - 130,236,685UniSTS
REN31098  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,661,526 - 132,661,777UniSTSGRCh37
Build 366132,703,219 - 132,703,470RGDNCBI36
Celera6133,408,411 - 133,408,661RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,236,632 - 130,236,883UniSTS
REN31099  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,662,081 - 132,662,321UniSTSGRCh37
Build 366132,703,774 - 132,704,014RGDNCBI36
Celera6133,408,965 - 133,409,205RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,237,187 - 130,237,427UniSTS
REN31100  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,662,317 - 132,662,542UniSTSGRCh37
Build 366132,704,010 - 132,704,235RGDNCBI36
Celera6133,409,201 - 133,409,426RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,237,423 - 130,237,648UniSTS
REN31101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,662,518 - 132,662,765UniSTSGRCh37
Build 366132,704,211 - 132,704,458RGDNCBI36
Celera6133,409,402 - 133,409,649RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,237,624 - 130,237,871UniSTS
REN31102  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,662,742 - 132,663,000UniSTSGRCh37
Build 366132,704,435 - 132,704,693RGDNCBI36
Celera6133,409,626 - 133,409,884RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,237,848 - 130,238,104UniSTS
REN31103  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,662,877 - 132,663,101UniSTSGRCh37
Build 366132,704,570 - 132,704,794RGDNCBI36
Celera6133,409,761 - 133,409,985RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,237,981 - 130,238,205UniSTS
REN31104  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,663,433 - 132,663,660UniSTSGRCh37
Build 366132,705,126 - 132,705,353RGDNCBI36
Celera6133,410,317 - 133,410,544RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,238,537 - 130,238,764UniSTS
REN31105  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,663,639 - 132,663,872UniSTSGRCh37
Build 366132,705,332 - 132,705,565RGDNCBI36
Celera6133,410,523 - 133,410,756RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,238,743 - 130,238,976UniSTS
REN31106  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,663,853 - 132,664,113UniSTSGRCh37
Build 366132,705,546 - 132,705,806RGDNCBI36
Celera6133,410,737 - 133,410,997RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,238,957 - 130,239,217UniSTS
REN31107  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,664,092 - 132,664,350UniSTSGRCh37
Build 366132,705,785 - 132,706,043RGDNCBI36
Celera6133,410,976 - 133,411,234RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,239,196 - 130,239,454UniSTS
REN31108  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,664,196 - 132,664,437UniSTSGRCh37
Build 366132,705,889 - 132,706,130RGDNCBI36
Celera6133,411,080 - 133,411,321RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,239,300 - 130,239,541UniSTS
REN31109  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,664,385 - 132,664,609UniSTSGRCh37
Build 366132,706,078 - 132,706,302RGDNCBI36
Celera6133,411,269 - 133,411,493RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,239,489 - 130,239,713UniSTS
REN31110  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,664,799 - 132,665,040UniSTSGRCh37
Build 366132,706,492 - 132,706,733RGDNCBI36
Celera6133,411,683 - 133,411,924RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,239,903 - 130,240,144UniSTS
REN31111  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,665,038 - 132,665,299UniSTSGRCh37
Build 366132,706,731 - 132,706,992RGDNCBI36
Celera6133,411,922 - 133,412,183RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,240,142 - 130,240,403UniSTS
REN31112  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,665,279 - 132,665,504UniSTSGRCh37
Build 366132,706,972 - 132,707,197RGDNCBI36
Celera6133,412,163 - 133,412,388RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,240,383 - 130,240,608UniSTS
REN31113  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,665,479 - 132,665,714UniSTSGRCh37
Build 366132,707,172 - 132,707,407RGDNCBI36
Celera6133,412,363 - 133,412,598RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,240,583 - 130,240,818UniSTS
REN31114  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,665,695 - 132,665,953UniSTSGRCh37
Build 366132,707,388 - 132,707,646RGDNCBI36
Celera6133,412,579 - 133,412,837RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,240,799 - 130,241,057UniSTS
REN31115  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,665,920 - 132,666,165UniSTSGRCh37
GRCh376132,665,920 - 132,666,143UniSTSGRCh37
Build 366132,707,613 - 132,707,836RGDNCBI36
Celera6133,412,804 - 133,413,049UniSTS
Celera6133,412,804 - 133,413,027RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,241,024 - 130,241,269UniSTS
REN31116  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,666,149 - 132,666,417UniSTSGRCh37
Build 366132,707,842 - 132,708,110RGDNCBI36
Celera6133,413,033 - 133,413,301RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,241,253 - 130,241,521UniSTS
REN31117  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,666,397 - 132,666,663UniSTSGRCh37
Build 366132,708,090 - 132,708,356RGDNCBI36
Celera6133,413,281 - 133,413,547RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,241,501 - 130,241,767UniSTS
REN31118  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,666,645 - 132,666,888UniSTSGRCh37
Build 366132,708,338 - 132,708,581RGDNCBI36
Celera6133,413,529 - 133,413,772RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,241,749 - 130,241,992UniSTS
REN31119  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,666,882 - 132,667,133UniSTSGRCh37
Build 366132,708,575 - 132,708,826RGDNCBI36
Celera6133,413,766 - 133,414,017RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,241,986 - 130,242,237UniSTS
REN31120  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,667,099 - 132,667,323UniSTSGRCh37
Build 366132,708,792 - 132,709,016RGDNCBI36
Celera6133,413,983 - 133,414,207RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,242,203 - 130,242,427UniSTS
REN31121  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,667,297 - 132,667,566UniSTSGRCh37
Build 366132,708,990 - 132,709,259RGDNCBI36
Celera6133,414,181 - 133,414,450RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,242,401 - 130,242,670UniSTS
REN31122  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,667,502 - 132,667,752UniSTSGRCh37
Build 366132,709,195 - 132,709,445RGDNCBI36
Celera6133,414,386 - 133,414,636RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,242,606 - 130,242,856UniSTS
REN31123  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,667,720 - 132,667,949UniSTSGRCh37
Build 366132,709,413 - 132,709,642RGDNCBI36
Celera6133,414,604 - 133,414,833RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,242,824 - 130,243,053UniSTS
REN31124  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,667,922 - 132,668,156UniSTSGRCh37
Build 366132,709,615 - 132,709,849RGDNCBI36
Celera6133,414,806 - 133,415,040RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,243,026 - 130,243,260UniSTS
REN31125  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,668,129 - 132,668,386UniSTSGRCh37
Build 366132,709,822 - 132,710,079RGDNCBI36
Celera6133,415,013 - 133,415,270RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,243,233 - 130,243,490UniSTS
REN31126  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,668,294 - 132,668,546UniSTSGRCh37
Build 366132,709,987 - 132,710,239RGDNCBI36
Celera6133,415,178 - 133,415,430RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,243,398 - 130,243,650UniSTS
REN31127  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,668,524 - 132,668,759UniSTSGRCh37
Build 366132,710,217 - 132,710,452RGDNCBI36
Celera6133,415,408 - 133,415,643RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,243,628 - 130,243,863UniSTS
REN31128  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,668,794 - 132,669,060UniSTSGRCh37
Build 366132,710,487 - 132,710,753RGDNCBI36
Celera6133,415,678 - 133,415,945RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,243,898 - 130,244,164UniSTS
REN31129  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,669,039 - 132,669,286UniSTSGRCh37
Build 366132,710,732 - 132,710,979RGDNCBI36
Celera6133,415,924 - 133,416,171RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,244,143 - 130,244,390UniSTS
REN31130  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,669,263 - 132,669,516UniSTSGRCh37
Build 366132,710,956 - 132,711,209RGDNCBI36
Celera6133,416,148 - 133,416,401RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,244,367 - 130,244,620UniSTS
REN31131  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,669,499 - 132,669,730UniSTSGRCh37
Build 366132,711,192 - 132,711,423RGDNCBI36
Celera6133,416,384 - 133,416,615RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,244,603 - 130,244,834UniSTS
REN31132  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,669,706 - 132,669,959UniSTSGRCh37
Build 366132,711,399 - 132,711,652RGDNCBI36
Celera6133,416,591 - 133,416,844RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,244,810 - 130,245,063UniSTS
REN31133  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,669,888 - 132,670,148UniSTSGRCh37
Build 366132,711,581 - 132,711,841RGDNCBI36
Celera6133,416,773 - 133,417,033RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,244,992 - 130,245,252UniSTS
REN31134  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,670,147 - 132,670,397UniSTSGRCh37
Build 366132,711,840 - 132,712,090RGDNCBI36
Celera6133,417,032 - 133,417,282RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,245,251 - 130,245,501UniSTS
REN31135  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,671,228 - 132,671,489UniSTSGRCh37
Build 366132,712,921 - 132,713,182RGDNCBI36
Celera6133,418,113 - 133,418,374RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,246,294 - 130,246,555UniSTS
REN31136  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,671,467 - 132,671,697UniSTSGRCh37
Build 366132,713,160 - 132,713,390RGDNCBI36
Celera6133,418,352 - 133,418,582RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,246,533 - 130,246,763UniSTS
REN31137  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,671,552 - 132,671,811UniSTSGRCh37
Build 366132,713,245 - 132,713,504RGDNCBI36
Celera6133,418,437 - 133,418,696RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,246,618 - 130,246,877UniSTS
REN31138  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,671,778 - 132,672,002UniSTSGRCh37
Build 366132,713,471 - 132,713,695RGDNCBI36
Celera6133,418,663 - 133,418,887RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,246,844 - 130,247,068UniSTS
REN31139  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,671,954 - 132,672,214UniSTSGRCh37
Build 366132,713,647 - 132,713,907RGDNCBI36
Celera6133,418,839 - 133,419,099RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,247,020 - 130,247,280UniSTS
REN31140  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,672,190 - 132,672,419UniSTSGRCh37
Build 366132,713,883 - 132,714,112RGDNCBI36
Celera6133,419,075 - 133,419,304RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,247,256 - 130,247,485UniSTS
REN31141  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,672,370 - 132,672,610UniSTSGRCh37
Build 366132,714,063 - 132,714,303RGDNCBI36
Celera6133,419,255 - 133,419,495RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,247,436 - 130,247,676UniSTS
REN31142  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,672,587 - 132,672,836UniSTSGRCh37
Build 366132,714,280 - 132,714,529RGDNCBI36
Celera6133,419,472 - 133,419,721RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,247,653 - 130,247,902UniSTS
REN31143  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,672,695 - 132,672,953UniSTSGRCh37
Build 366132,714,388 - 132,714,646RGDNCBI36
Celera6133,419,580 - 133,419,838RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,247,761 - 130,248,019UniSTS
REN31144  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,672,860 - 132,673,126UniSTSGRCh37
Build 366132,714,553 - 132,714,819RGDNCBI36
Celera6133,419,745 - 133,420,011RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,247,926 - 130,248,192UniSTS
REN31145  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,673,050 - 132,673,289UniSTSGRCh37
Build 366132,714,743 - 132,714,982RGDNCBI36
Celera6133,419,935 - 133,420,174RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,248,116 - 130,248,355UniSTS
REN31146  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,673,246 - 132,673,472UniSTSGRCh37
Build 366132,714,939 - 132,715,165RGDNCBI36
Celera6133,420,131 - 133,420,357RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,248,312 - 130,248,538UniSTS
REN31147  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,673,366 - 132,673,594UniSTSGRCh37
Build 366132,715,059 - 132,715,287RGDNCBI36
Celera6133,420,251 - 133,420,479RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,248,432 - 130,248,660UniSTS
REN31148  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,673,675 - 132,673,899UniSTSGRCh37
Build 366132,715,368 - 132,715,592RGDNCBI36
Celera6133,420,560 - 133,420,784RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,248,741 - 130,248,965UniSTS
REN31150  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,674,038 - 132,674,279UniSTSGRCh37
Build 366132,715,731 - 132,715,972RGDNCBI36
Celera6133,420,923 - 133,421,164RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,249,104 - 130,249,345UniSTS
REN31151  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,674,256 - 132,674,507UniSTSGRCh37
Build 366132,715,949 - 132,716,200RGDNCBI36
Celera6133,421,141 - 133,421,392RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,249,322 - 130,249,573UniSTS
REN31152  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,674,478 - 132,674,724UniSTSGRCh37
Build 366132,716,171 - 132,716,417RGDNCBI36
Celera6133,421,363 - 133,421,609RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,249,544 - 130,249,790UniSTS
REN31153  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,674,708 - 132,674,974UniSTSGRCh37
Build 366132,716,401 - 132,716,667RGDNCBI36
Celera6133,421,593 - 133,421,859RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,249,774 - 130,250,040UniSTS
REN31154  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,674,973 - 132,675,239UniSTSGRCh37
Build 366132,716,666 - 132,716,932RGDNCBI36
Celera6133,421,858 - 133,422,124RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,250,039 - 130,250,305UniSTS
REN31155  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,675,218 - 132,675,457UniSTSGRCh37
Build 366132,716,911 - 132,717,150RGDNCBI36
Celera6133,422,103 - 133,422,342RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,250,284 - 130,250,523UniSTS
REN31156  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,675,434 - 132,675,684UniSTSGRCh37
Build 366132,717,127 - 132,717,377RGDNCBI36
Celera6133,422,319 - 133,422,569RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,250,500 - 130,250,750UniSTS
REN31157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,675,637 - 132,675,888UniSTSGRCh37
Build 366132,717,330 - 132,717,581RGDNCBI36
Celera6133,422,522 - 133,422,773RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,250,703 - 130,250,954UniSTS
REN31158  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,675,853 - 132,676,090UniSTSGRCh37
Build 366132,717,546 - 132,717,783RGDNCBI36
Celera6133,422,738 - 133,422,975RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,250,919 - 130,251,156UniSTS
REN31159  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,676,067 - 132,676,330UniSTSGRCh37
Build 366132,717,760 - 132,718,023RGDNCBI36
Celera6133,422,952 - 133,423,215RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,251,133 - 130,251,396UniSTS
REN31160  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,676,329 - 132,676,583UniSTSGRCh37
Build 366132,718,022 - 132,718,276RGDNCBI36
Celera6133,423,214 - 133,423,468RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,251,395 - 130,251,649UniSTS
REN31161  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,676,570 - 132,676,830UniSTSGRCh37
Build 366132,718,263 - 132,718,523RGDNCBI36
Celera6133,423,455 - 133,423,715RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,251,636 - 130,251,896UniSTS
REN31162  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,676,809 - 132,677,045UniSTSGRCh37
Build 366132,718,502 - 132,718,738RGDNCBI36
Celera6133,423,694 - 133,423,930RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,251,875 - 130,252,111UniSTS
REN31163  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,676,890 - 132,677,139UniSTSGRCh37
Build 366132,718,583 - 132,718,832RGDNCBI36
Celera6133,423,775 - 133,424,024RGD
Cytogenetic Map6q23.2UniSTS
HuRef6130,251,956 - 130,252,205UniSTS
stSG626642  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,632,974 - 132,634,291UniSTSGRCh37
Build 366132,674,667 - 132,675,984RGDNCBI36
Celera6133,379,856 - 133,381,173RGD
HuRef6130,208,068 - 130,209,385UniSTS
stSG626643  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,633,576 - 132,634,628UniSTSGRCh37
Build 366132,675,269 - 132,676,321RGDNCBI36
Celera6133,380,458 - 133,381,510RGD
HuRef6130,208,670 - 130,209,722UniSTS
stSG626644  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,636,623 - 132,636,919UniSTSGRCh37
Build 366132,678,316 - 132,678,612RGDNCBI36
Celera6133,383,505 - 133,383,801RGD
HuRef6130,211,717 - 130,212,013UniSTS
stSG626645  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,637,134 - 132,638,456UniSTSGRCh37
Build 366132,678,827 - 132,680,149RGDNCBI36
Celera6133,384,016 - 133,385,339RGD
HuRef6130,212,228 - 130,213,550UniSTS
stSG626646  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,640,705 - 132,641,810UniSTSGRCh37
Build 366132,682,398 - 132,683,503RGDNCBI36
Celera6133,387,588 - 133,388,693RGD
HuRef6130,215,799 - 130,216,904UniSTS
stSG626647  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,641,921 - 132,643,106UniSTSGRCh37
Build 366132,683,614 - 132,684,799RGDNCBI36
Celera6133,388,804 - 133,389,989RGD
HuRef6130,217,015 - 130,218,200UniSTS
stSG626648  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,643,090 - 132,644,204UniSTSGRCh37
Build 366132,684,783 - 132,685,897RGDNCBI36
Celera6133,389,973 - 133,391,087RGD
HuRef6130,218,184 - 130,219,298UniSTS
stSG626649  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,644,185 - 132,645,476UniSTSGRCh37
Build 366132,685,878 - 132,687,169RGDNCBI36
Celera6133,391,068 - 133,392,359RGD
HuRef6130,219,279 - 130,220,570UniSTS
stSG626650  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,645,370 - 132,646,372UniSTSGRCh37
Build 366132,687,063 - 132,688,065RGDNCBI36
Celera6133,392,253 - 133,393,257RGD
HuRef6130,220,464 - 130,221,468UniSTS
stSG626651  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,646,252 - 132,647,265UniSTSGRCh37
Build 366132,687,945 - 132,688,958RGDNCBI36
Celera6133,393,137 - 133,394,150RGD
HuRef6130,221,348 - 130,222,361UniSTS
stSG626652  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,647,247 - 132,648,305UniSTSGRCh37
Build 366132,688,940 - 132,689,998RGDNCBI36
Celera6133,394,132 - 133,395,190RGD
HuRef6130,222,343 - 130,223,401UniSTS
stSG626653  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,648,286 - 132,649,633UniSTSGRCh37
Build 366132,689,979 - 132,691,326RGDNCBI36
Celera6133,395,171 - 133,396,518RGD
HuRef6130,223,382 - 130,224,729UniSTS
stSG626654  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,649,614 - 132,651,086UniSTSGRCh37
Build 366132,691,307 - 132,692,779RGDNCBI36
Celera6133,396,499 - 133,397,971RGD
HuRef6130,224,710 - 130,226,182UniSTS
stSG626655  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,651,072 - 132,652,328UniSTSGRCh37
Build 366132,692,765 - 132,694,021RGDNCBI36
Celera6133,397,957 - 133,399,213RGD
HuRef6130,226,168 - 130,227,424UniSTS
stSG626656  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,652,309 - 132,653,684UniSTSGRCh37
Build 366132,694,002 - 132,695,377RGDNCBI36
Celera6133,399,194 - 133,400,569RGD
HuRef6130,227,405 - 130,228,780UniSTS
stSG626657  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,653,830 - 132,655,165UniSTSGRCh37
Build 366132,695,523 - 132,696,858RGDNCBI36
Celera6133,400,715 - 133,402,050RGD
HuRef6130,228,926 - 130,230,271UniSTS
stSG626658  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,655,146 - 132,656,288UniSTSGRCh37
Build 366132,696,839 - 132,697,981RGDNCBI36
Celera6133,402,031 - 133,403,173RGD
HuRef6130,230,252 - 130,231,394UniSTS
stSG626659  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,656,269 - 132,657,426UniSTSGRCh37
Build 366132,697,962 - 132,699,119RGDNCBI36
Celera6133,403,154 - 133,404,311RGD
HuRef6130,231,375 - 130,232,532UniSTS
stSG626660  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,657,407 - 132,658,494UniSTSGRCh37
Build 366132,699,100 - 132,700,187RGDNCBI36
Celera6133,404,292 - 133,405,379RGD
HuRef6130,232,513 - 130,233,600UniSTS
stSG626661  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,658,475 - 132,659,549UniSTSGRCh37
Build 366132,700,168 - 132,701,242RGDNCBI36
Celera6133,405,360 - 133,406,434RGD
HuRef6130,233,581 - 130,234,655UniSTS
stSG626662  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,659,528 - 132,660,896UniSTSGRCh37
Build 366132,701,221 - 132,702,589RGDNCBI36
Celera6133,406,413 - 133,407,781RGD
HuRef6130,234,634 - 130,236,002UniSTS
stSG626663  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,660,714 - 132,661,718UniSTSGRCh37
Build 366132,702,407 - 132,703,411RGDNCBI36
Celera6133,407,599 - 133,408,602RGD
HuRef6130,235,820 - 130,236,824UniSTS
stSG626664  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,661,697 - 132,662,993UniSTSGRCh37
Build 366132,703,390 - 132,704,686RGDNCBI36
Celera6133,408,581 - 133,409,877RGD
HuRef6130,236,803 - 130,238,097UniSTS
stSG626665  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,662,973 - 132,663,997UniSTSGRCh37
Build 366132,704,666 - 132,705,690RGDNCBI36
Celera6133,409,857 - 133,410,881RGD
HuRef6130,238,077 - 130,239,101UniSTS
stSG626666  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,664,030 - 132,665,403UniSTSGRCh37
Build 366132,705,723 - 132,707,096RGDNCBI36
Celera6133,410,914 - 133,412,287RGD
HuRef6130,239,134 - 130,240,507UniSTS
stSG626667  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,665,387 - 132,666,875UniSTSGRCh37
Build 366132,707,080 - 132,708,568RGDNCBI36
Celera6133,412,271 - 133,413,759RGD
HuRef6130,240,491 - 130,241,979UniSTS
stSG626668  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,667,005 - 132,668,091UniSTSGRCh37
Build 366132,708,698 - 132,709,784RGDNCBI36
Celera6133,413,889 - 133,414,975RGD
HuRef6130,242,109 - 130,243,195UniSTS
stSG626669  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,668,382 - 132,669,530UniSTSGRCh37
Build 366132,710,075 - 132,711,223RGDNCBI36
Celera6133,415,266 - 133,416,415RGD
HuRef6130,243,486 - 130,244,634UniSTS
stSG626670  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376132,669,064 - 132,670,086UniSTSGRCh37
Build 366132,710,757 - 132,711,779RGDNCBI36
Celera6133,415,949 - 133,416,971RGD
HuRef6130,244,168 - 130,245,190UniSTS
D6S413  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map6q23.2UniSTS
D6S413  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map6q23.2UniSTS
Marshfield Genetic Map6131.07UniSTS
Genethon Genetic Map6131.5UniSTS
deCODE Assembly Map6131.33UniSTS
GeneMap99-GB4 RH Map6532.92UniSTS
Whitehead-RH Map6756.1UniSTS
Whitehead-YAC Contig Map6 UniSTS
NCBI RH Map61538.9UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
pharyngeal arch
renal system
reproductive system
respiratory system
sensory system
visual system
1204 2371 2768 2245 4959 1712 2300 3 615 1839 456 2264 7106 6351 45 3721 1 845 1733 1575 173 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_015529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017010714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047418621 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047418622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054355127 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054355128 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054355129 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AI751100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ420565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074879 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK226054 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL023578 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL080058 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL357034 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY007239 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY359094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC018756 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Ensembl Acc Id: ENST00000336749   ⟹   ENSP00000336998
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6132,296,069 - 132,375,065 (-)Ensembl
Ensembl Acc Id: ENST00000367963   ⟹   ENSP00000356940
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6132,296,055 - 132,401,475 (-)Ensembl
Ensembl Acc Id: ENST00000392401   ⟹   ENSP00000376202
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6132,390,422 - 132,401,475 (-)Ensembl
Ensembl Acc Id: ENST00000489128
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6132,315,697 - 132,325,147 (-)Ensembl
RefSeq Acc Id: NM_015529   ⟹   NP_056344
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386132,296,055 - 132,401,475 (-)NCBI
GRCh376132,617,194 - 132,722,664 (-)RGD
Build 366132,658,887 - 132,764,357 (-)NCBI Archive
Celera6133,364,075 - 133,469,523 (-)RGD
HuRef6130,192,320 - 130,297,382 (-)ENTREZGENE
CHM1_16132,880,907 - 132,986,349 (-)NCBI
T2T-CHM13v2.06133,491,085 - 133,596,465 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017010714   ⟹   XP_016866203
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386132,296,055 - 132,401,475 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047418621   ⟹   XP_047274577
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386132,296,055 - 132,386,504 (-)NCBI
RefSeq Acc Id: XM_047418622   ⟹   XP_047274578
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386132,296,055 - 132,392,259 (-)NCBI
RefSeq Acc Id: XM_054355127   ⟹   XP_054211102
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06133,491,085 - 133,596,511 (-)NCBI
RefSeq Acc Id: XM_054355128   ⟹   XP_054211103
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06133,491,085 - 133,581,489 (-)NCBI
RefSeq Acc Id: XM_054355129   ⟹   XP_054211104
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06133,491,085 - 133,587,244 (-)NCBI
RefSeq Acc Id: NP_056344   ⟸   NM_015529
- Peptide Label: precursor
- UniProtKB: Q9H4M6 (UniProtKB/Swiss-Prot),   Q8WV49 (UniProtKB/Swiss-Prot),   Q8NC97 (UniProtKB/Swiss-Prot),   Q5THU6 (UniProtKB/Swiss-Prot),   Q9Y4U3 (UniProtKB/Swiss-Prot),   Q6UVY6 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_016866203   ⟸   XM_017010714
- Peptide Label: isoform X1
- Sequence:
Ensembl Acc Id: ENSP00000336998   ⟸   ENST00000336749
Ensembl Acc Id: ENSP00000376202   ⟸   ENST00000392401
Ensembl Acc Id: ENSP00000356940   ⟸   ENST00000367963
RefSeq Acc Id: XP_047274578   ⟸   XM_047418622
- Peptide Label: isoform X3
RefSeq Acc Id: XP_047274577   ⟸   XM_047418621
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054211102   ⟸   XM_054355127
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054211104   ⟸   XM_054355129
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054211103   ⟸   XM_054355128
- Peptide Label: isoform X2
Protein Domains
DOMON

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q6UVY6-F1-model_v2 AlphaFold Q6UVY6 1-613 view protein structure

Promoters
RGD ID:7209169
Promoter ID:EPDNEW_H10329
Type:initiation region
Name:MOXD1_1
Description:monooxygenase DBH like 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10330  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh386132,401,475 - 132,401,535EPDNEW
RGD ID:7209167
Promoter ID:EPDNEW_H10330
Type:initiation region
Name:MOXD1_2
Description:monooxygenase DBH like 1
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H10329  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh386132,402,072 - 132,402,132EPDNEW
RGD ID:6804001
Promoter ID:HG_KWN:55038
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Lymphoblastoid
Transcripts:ENST00000392401,   OTTHUMT00000125837
Position:
Human AssemblyChrPosition (strand)Source
Build 366132,764,049 - 132,764,549 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:21063 AgrOrtholog
COSMIC MOXD1 COSMIC
Ensembl Genes ENSG00000079931 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000336749 ENTREZGENE
  ENST00000336749.3 UniProtKB/Swiss-Prot
  ENST00000367963 ENTREZGENE
  ENST00000367963.8 UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.120.230 UniProtKB/Swiss-Prot
  2.60.120.310 UniProtKB/Swiss-Prot
GTEx ENSG00000079931 GTEx
HGNC ID HGNC:21063 ENTREZGENE
Human Proteome Map MOXD1 Human Proteome Map
InterPro Cu2_ascorb_mOase-like_C UniProtKB/Swiss-Prot
  Cu2_ascorb_mOase_N UniProtKB/Swiss-Prot
  Cu2_ascorb_mOase_N_sf UniProtKB/Swiss-Prot
  Cu2_monoox_C UniProtKB/Swiss-Prot
  DBH-like UniProtKB/Swiss-Prot
  DOH_DOMON UniProtKB/Swiss-Prot
  DOMON_domain UniProtKB/Swiss-Prot
  PHM/PNGase_F_dom_sf UniProtKB/Swiss-Prot
  Tbh/DBH UniProtKB/Swiss-Prot
KEGG Report hsa:26002 UniProtKB/Swiss-Prot
NCBI Gene 26002 ENTREZGENE
OMIM 609000 OMIM
PANTHER PTHR10157 UniProtKB/Swiss-Prot
  PTHR10157:SF28 UniProtKB/Swiss-Prot
Pfam Cu2_monoox_C UniProtKB/Swiss-Prot
  Cu2_monooxygen UniProtKB/Swiss-Prot
  DOMON UniProtKB/Swiss-Prot
PharmGKB PA134979178 PharmGKB
PRINTS DBMONOXGNASE UniProtKB/Swiss-Prot
PROSITE DOMON UniProtKB/Swiss-Prot
SMART DoH UniProtKB/Swiss-Prot
Superfamily-SCOP SSF49742 UniProtKB/Swiss-Prot
UniProt A6PVS1_HUMAN UniProtKB/TrEMBL
  MOXD1_HUMAN UniProtKB/Swiss-Prot
  Q5THU6 ENTREZGENE
  Q6UVY6 ENTREZGENE
  Q8NC97 ENTREZGENE
  Q8WV49 ENTREZGENE
  Q9H4M6 ENTREZGENE
  Q9Y4U3 ENTREZGENE
UniProt Secondary Q5THU6 UniProtKB/Swiss-Prot
  Q8NC97 UniProtKB/Swiss-Prot
  Q8WV49 UniProtKB/Swiss-Prot
  Q9H4M6 UniProtKB/Swiss-Prot
  Q9Y4U3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-04-12 MOXD1  monooxygenase DBH like 1    monooxygenase, DBH-like 1  Symbol and/or name change 5135510 APPROVED