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Gene: MIR9-3HG (MIR9-3 host gene) Homo sapiens

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Symbol:

MIR9-3HG

Name:

MIR9-3 host gene

RGD ID:

7244794

HGNC Page

HGNC:27388

Description:

INTERACTS WITH 4,4'-sulfonyldiphenol; acrylamide; aflatoxin B1

Type:

ncrna (Ensembl: lncRNA)

RefSeq Status:

VALIDATED

Previously known as:

BS-DRL1; LINC00925; lnc-FANCI-2

RGD Orthologs

Mouse

Alliance Orthologs

More Info

more info ...

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	15	89,361,579 - 89,398,488 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	15	89,361,579 - 89,424,983 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	15	89,904,810 - 89,941,719 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Celera	15	66,323,662 - 66,344,098 (+)	NCBI		Celera
Cytogenetic Map	15	q26.1	NCBI
HuRef	15	66,034,099 - 66,054,595 (+)	NCBI		HuRef
CHM1_1	15	89,762,283 - 89,782,728 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	15	87,117,636 - 87,154,521 (+)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

2,3,7,8-tetrachlorodibenzodioxine (ISO)

4,4'-sulfonyldiphenol (EXP)

acrylamide (EXP)

aflatoxin B1 (EXP)

all-trans-retinoic acid (ISO)

aristolochic acid A (EXP)

benzo[a]pyrene (EXP)

benzo[e]pyrene (EXP)

bisphenol A (EXP,ISO)

bisphenol F (ISO)

butanal (EXP)

ethanol (ISO)

methapyrilene (EXP)

sodium arsenite (EXP)

valproic acid (EXP)

References

References - curated

#	Reference Title	Reference Citation
1.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:12477932	PMID:14702039	PMID:15701730	PMID:16344560	PMID:28397066	PMID:31938968	PMID:33436409	PMID:33596784	PMID:34210972	PMID:34468010	PMID:35933883	PMID:36408157

Genomics

Comparative Map Data

MIR9-3HG
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	15	89,361,579 - 89,398,488 (+)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	15	89,361,579 - 89,424,983 (+)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	15	89,904,810 - 89,941,719 (+)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Celera	15	66,323,662 - 66,344,098 (+)	NCBI		Celera
Cytogenetic Map	15	q26.1	NCBI
HuRef	15	66,034,099 - 66,054,595 (+)	NCBI		HuRef
CHM1_1	15	89,762,283 - 89,782,728 (+)	NCBI		CHM1_1
T2T-CHM13v2.0	15	87,117,636 - 87,154,521 (+)	NCBI		T2T-CHM13v2.0

Mir9-3hg
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	7	79,149,774 - 79,184,151 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	7	79,146,444 - 79,184,154 (+)	Ensembl		GRCm39 Ensembl
GRCm38	7	79,500,026 - 79,534,403 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	7	79,500,026 - 79,534,403 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	7	86,644,924 - 86,679,289 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	7	79,372,593 - 79,406,104 (+)	NCBI		MGSCv36	mm8
Celera	7	76,903,810 - 76,938,181 (+)	NCBI		Celera
Cytogenetic Map	7	D2	NCBI
cM Map	7	45.06	NCBI

Variants

Variants in MIR9-3HG
7 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 15q25.2-26.3(chr15:83711377-101843270)x3	copy number gain	See cases [RCV000135858]	Chr15:83711377..101843270 [GRCh38] Chr15:84380129..102383473 [GRCh37] Chr15:82171133..100200996 [NCBI36] Chr15:15q25.2-26.3	pathogenic
GRCh38/hg38 15q25.3-26.3(chr15:87904735-101843270)x3	copy number gain	See cases [RCV000135568]	Chr15:87904735..101843270 [GRCh38] Chr15:88447966..102383473 [GRCh37] Chr15:86248970..100200996 [NCBI36] Chr15:15q25.3-26.3	pathogenic
GRCh38/hg38 15q25.2-26.3(chr15:82859676-101810992)x3	copy number gain	See cases [RCV000136849]	Chr15:82859676..101810992 [GRCh38] Chr15:83528428..102351195 [GRCh37] Chr15:81325482..100168718 [NCBI36] Chr15:15q25.2-26.3	pathogenic
GRCh38/hg38 15q25.3-26.3(chr15:85826665-101920998)x4	copy number gain	See cases [RCV000137264]	Chr15:85826665..101920998 [GRCh38] Chr15:86369896..102461201 [GRCh37] Chr15:84170900..100278724 [NCBI36] Chr15:15q25.3-26.3	pathogenic
GRCh38/hg38 15q25.3-26.3(chr15:85397539-101888909)x3	copy number gain	See cases [RCV000141899]	Chr15:85397539..101888909 [GRCh38] Chr15:85940770..102429112 [GRCh37] Chr15:83741774..100246635 [NCBI36] Chr15:15q25.3-26.3	pathogenic
GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3	copy number gain	See cases [RCV000143019]	Chr15:72154949..101920998 [GRCh38] Chr15:72447290..102461201 [GRCh37] Chr15:70234344..100278724 [NCBI36] Chr15:15q23-26.3	pathogenic
GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3	copy number gain	See cases [RCV000142915]	Chr15:59828460..101920998 [GRCh38] Chr15:60120659..102461201 [GRCh37] Chr15:57907951..100278724 [NCBI36] Chr15:15q22.2-26.3	pathogenic
GRCh38/hg38 15q26.1-26.3(chr15:88676575-98364743)x3	copy number gain	See cases [RCV000142727]	Chr15:88676575..98364743 [GRCh38] Chr15:89219806..98907972 [GRCh37] Chr15:87020810..96725495 [NCBI36] Chr15:15q26.1-26.3	pathogenic
GRCh38/hg38 15q24.2-26.3(chr15:75307767-101723215)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052346]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052346]\|See cases [RCV000052346]	Chr15:75307767..101723215 [GRCh38] Chr15:75600108..102263418 [GRCh37] Chr15:73387161..100080941 [NCBI36] Chr15:15q24.2-26.3	pathogenic
GRCh38/hg38 15q24.3-26.3(chr15:77543797-101843411)x3	copy number gain	See cases [RCV000052347]	Chr15:77543797..101843411 [GRCh38] Chr15:77836139..102383614 [GRCh37] Chr15:75623194..100201137 [NCBI36] Chr15:15q24.3-26.3	pathogenic
GRCh38/hg38 15q25.2-26.3(chr15:84169153-101904929)x3	copy number gain	See cases [RCV000052352]	Chr15:84169153..101904929 [GRCh38] Chr15:84837905..102445132 [GRCh37] Chr15:82628909..100262655 [NCBI36] Chr15:15q25.2-26.3	pathogenic

miRNA Target Status (No longer updated)

Predicted Target Of

	Summary Value
Count of predictions:	2488
Count of miRNA genes:	803
Interacting mature miRNAs:	943
Transcripts:	ENST00000536780, ENST00000538734, ENST00000546186, ENST00000558692, ENST00000558754, ENST00000558982, ENST00000559235, ENST00000560008, ENST00000560596, ENST00000560663, ENST00000561037, ENST00000561327
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.

RGD ID	Symbol	Name	LOD	P Value	Trait	Sub Trait	Chr	Start	Stop	Species
596973847	GWAS1093366_H	memory performance QTL GWAS1093366 (human)		0.000006	memory performance		15	89362349	89362350	Human
597463967	GWAS1560041_H	diet measurement QTL GWAS1560041 (human)		4e-09	eating behavior trait (VT:0001431)	food intake measurement (CMO:0000772)	15	89369267	89369268	Human
597500958	GWAS1597032_H	retinal drusen QTL GWAS1597032 (human)		0.000005	retinal drusen		15	89387917	89387918	Human
597367699	GWAS1463773_H	insomnia measurement QTL GWAS1463773 (human)		9e-09	sleep behavior trait (VT:0001501)		15	89370401	89370402	Human
597498700	GWAS1594774_H	memory performance QTL GWAS1594774 (human)		0.000005	memory performance		15	89362349	89362350	Human
597461513	GWAS1557587_H	smoking status measurement QTL GWAS1557587 (human)		3e-08	smoking status measurement		15	89370401	89370402	Human
596980162	GWAS1099681_H	memory performance QTL GWAS1099681 (human)		0.000005	memory performance		15	89362349	89362350	Human
597368643	GWAS1464717_H	insomnia measurement QTL GWAS1464717 (human)		1e-09	sleep behavior trait (VT:0001501)		15	89378738	89378739	Human
597497988	GWAS1594062_H	memory performance QTL GWAS1594062 (human)		0.000006	memory performance		15	89362349	89362350	Human
597381504	GWAS1477578_H	fat body mass QTL GWAS1477578 (human)		0.000005	body fat mass (VT:0010482)	total body fat mass (CMO:0000305)	15	89388485	89388486	Human
597492160	GWAS1588234_H	insomnia QTL GWAS1588234 (human)		2e-08	insomnia		15	89370401	89370402	Human
597497661	GWAS1593735_H	retinal drusen QTL GWAS1593735 (human)		0.00001	retinal drusen		15	89396297	89396298	Human
597479485	GWAS1575559_H	biological sex QTL GWAS1575559 (human)		3e-09	biological sex		15	89376714	89376715	Human
597497660	GWAS1593734_H	retinal drusen QTL GWAS1593734 (human)		0.000002	retinal drusen		15	89387917	89387918	Human
597515384	GWAS1611458_H	body mass index QTL GWAS1611458 (human)		9e-13	body mass index	body mass index (BMI) (CMO:0000105)	15	89384958	89384959	Human
597497979	GWAS1594053_H	lean body mass QTL GWAS1594053 (human)		1e-11	body lean mass (VT:0010483)	total body lean mass (CMO:0003950)	15	89384958	89384959	Human
597524597	GWAS1620671_H	smoking initiation QTL GWAS1620671 (human)		1e-16	smoking initiation		15	89383568	89383569	Human
597464756	GWAS1560830_H	tobacco smoke exposure measurement QTL GWAS1560830 (human)		3e-08	tobacco smoke exposure measurement		15	89384958	89384959	Human
597391729	GWAS1487803_H	smoking behavior QTL GWAS1487803 (human)		3e-09	smoking behavior		15	89370401	89370402	Human
597368817	GWAS1464891_H	white matter microstructure measurement QTL GWAS1464891 (human)		5e-11	white matter microstructure measurement		15	89376714	89376715	Human
597471415	GWAS1567489_H	appendicular lean mass QTL GWAS1567489 (human)		1e-12	appendicular lean mass		15	89361921	89361922	Human
597408245	GWAS1504319_H	body mass index QTL GWAS1504319 (human)		6e-10	body mass index	body mass index (BMI) (CMO:0000105)	15	89384958	89384959	Human
596953313	GWAS1072832_H	smoking behaviour measurement, risk-taking behaviour QTL GWAS1072832 (human)		3e-09	smoking behaviour measurement, risk-taking behaviour		15	89387917	89387918	Human
597399340	GWAS1495414_H	schizophrenia QTL GWAS1495414 (human)		0.0000001	schizophrenia		15	89384958	89384959	Human
597408352	GWAS1504426_H	Stuttering QTL GWAS1504426 (human)		0.000002	Stuttering		15	89384284	89384285	Human
597366501	GWAS1462575_H	white matter microstructure measurement QTL GWAS1462575 (human)		9e-10	white matter microstructure measurement		15	89376714	89376715	Human
597380133	GWAS1476207_H	smoking status measurement QTL GWAS1476207 (human)		4e-09	smoking status measurement		15	89387917	89387918	Human
597388517	GWAS1484591_H	fat body mass QTL GWAS1484591 (human)		0.000006	body fat mass (VT:0010482)	total body fat mass (CMO:0000305)	15	89388485	89388486	Human

Markers in Region

D15S1498

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	15	89,924,456 - 89,924,581	UniSTS	GRCh37
Build 36	15	87,725,460 - 87,725,585	RGD	NCBI36
Celera	15	66,326,845 - 66,326,970	RGD
Cytogenetic Map	15	q26.1	UniSTS
HuRef	15	66,037,282 - 66,037,407	UniSTS

Expression

RNA-SEQ Expression

Click on a value in the shaded box below the category label to view a detailed expression data table for that system.

Download All Expressed Objects for this Gene

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	renal system	reproductive system	respiratory system	sensory system	visual system
1171	2296	2576	2184	4865	1595	2151	5	514	1701	353	2179	6596	6127	31	3664	789	1680	1529	171	1

Sequence

Nucleotide Sequences


RefSeq Transcripts	NR_015411	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_133001	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_133002	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_133003	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190290	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190291	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190292	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190293	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190294	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190295	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190296	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190297	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190298	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190299	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190300	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190301	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190302	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190303	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190304	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190305	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190306	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190307	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190308	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190309	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190310	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190311	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190312	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190313	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190314	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190315	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190316	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190317	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190318	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190319	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190320	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190321	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190322	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190323	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190324	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190325	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NR_190326	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AC013391	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC133637	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK054710	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK054931	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK096359	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK123792	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK125292	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL520041	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL520042	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL526389	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AL526577	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC033240	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BX441353	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068263	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA059714	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB020558	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB067527	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB068800	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB452761	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB454083	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669800	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669801	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669802	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669803	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669804	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669805	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669806	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669807	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669808	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669809	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669810	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669811	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669812	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	MT669813	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

Ensembl Acc Id:

ENST00000536780

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,361,579 - 89,398,487 (+)	Ensembl

Ensembl Acc Id:

ENST00000538734

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,379,233 - 89,396,468 (+)	Ensembl

Ensembl Acc Id:

ENST00000546186

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,379,332 - 89,396,413 (+)	Ensembl

Ensembl Acc Id:

ENST00000558692

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,377,955 - 89,395,351 (+)	Ensembl

Ensembl Acc Id:

ENST00000558754

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,378,563 - 89,396,795 (+)	Ensembl

Ensembl Acc Id:

ENST00000558982

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,379,124 - 89,395,119 (+)	Ensembl

Ensembl Acc Id:

ENST00000559235

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,377,944 - 89,395,357 (+)	Ensembl

Ensembl Acc Id:

ENST00000560596

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,371,985 - 89,395,350 (+)	Ensembl

Ensembl Acc Id:

ENST00000560663

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,369,155 - 89,387,843 (+)	Ensembl

Ensembl Acc Id:

ENST00000561037

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,500 - 89,395,040 (+)	Ensembl

Ensembl Acc Id:

ENST00000561327

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,362,487 - 89,395,331 (+)	Ensembl

Ensembl Acc Id:

ENST00000654079

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,368,082 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000654171

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,362,474 - 89,398,485 (+)	Ensembl

Ensembl Acc Id:

ENST00000654184

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,362,509 - 89,398,485 (+)	Ensembl

Ensembl Acc Id:

ENST00000655673

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,369,099 - 89,395,350 (+)	Ensembl

Ensembl Acc Id:

ENST00000655914

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,474 - 89,389,522 (+)	Ensembl

Ensembl Acc Id:

ENST00000656907

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,369,103 - 89,395,349 (+)	Ensembl

Ensembl Acc Id:

ENST00000657897

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,362,509 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000658194

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,362,516 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000658764

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,368,212 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000658770

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,371,604 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000659235

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,362,662 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000659850

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,369,114 - 89,395,350 (+)	Ensembl

Ensembl Acc Id:

ENST00000660601

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,379,262 - 89,396,468 (+)	Ensembl

Ensembl Acc Id:

ENST00000660922

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,379,299 - 89,396,464 (+)	Ensembl

Ensembl Acc Id:

ENST00000661036

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,362,517 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000661040

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,362,509 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000662043

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,369,121 - 89,395,998 (+)	Ensembl

Ensembl Acc Id:

ENST00000662136

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,474 - 89,396,457 (+)	Ensembl

Ensembl Acc Id:

ENST00000662152

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,377,944 - 89,389,522 (+)	Ensembl

Ensembl Acc Id:

ENST00000662255

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,483 - 89,395,350 (+)	Ensembl

Ensembl Acc Id:

ENST00000662942

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,369,121 - 89,395,350 (+)	Ensembl

Ensembl Acc Id:

ENST00000663717

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,386,711 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000664345

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,483 - 89,395,357 (+)	Ensembl

Ensembl Acc Id:

ENST00000664499

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,474 - 89,395,362 (+)	Ensembl

Ensembl Acc Id:

ENST00000664594

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,504 - 89,395,351 (+)	Ensembl

Ensembl Acc Id:

ENST00000664925

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,474 - 89,395,351 (+)	Ensembl

Ensembl Acc Id:

ENST00000665086

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,379,585 - 89,395,337 (+)	Ensembl

Ensembl Acc Id:

ENST00000665619

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,377,938 - 89,395,359 (+)	Ensembl

Ensembl Acc Id:

ENST00000665852

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,377,969 - 89,395,990 (+)	Ensembl

Ensembl Acc Id:

ENST00000666816

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,371,603 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000667285

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,377,739 - 89,396,468 (+)	Ensembl

Ensembl Acc Id:

ENST00000667575

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,474 - 89,395,351 (+)	Ensembl

Ensembl Acc Id:

ENST00000668524

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,377,920 - 89,396,468 (+)	Ensembl

Ensembl Acc Id:

ENST00000669037

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,369,125 - 89,395,359 (+)	Ensembl

Ensembl Acc Id:

ENST00000669098

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,378,966 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000669499

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,362,686 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000669645

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,379,251 - 89,396,463 (+)	Ensembl

Ensembl Acc Id:

ENST00000670238

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,379,302 - 89,396,466 (+)	Ensembl

Ensembl Acc Id:

ENST00000670485

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,382,497 - 89,395,086 (+)	Ensembl

Ensembl Acc Id:

ENST00000670779

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,368,141 - 89,398,487 (+)	Ensembl

Ensembl Acc Id:

ENST00000671075

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,386,464 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000671447

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,387,332 - 89,398,484 (+)	Ensembl

Ensembl Acc Id:

ENST00000701636

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	15	89,378,121 - 89,424,983 (+)	Ensembl

RefSeq Acc Id:

NR_015411

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,104 - 89,398,488 (+)	NCBI
GRCh37	15	89,921,273 - 89,941,718 (+)	NCBI
HuRef	15	66,034,099 - 66,054,595 (+)	NCBI
CHM1_1	15	89,762,283 - 89,782,728 (+)	NCBI
T2T-CHM13v2.0	15	87,134,136 - 87,154,521 (+)	NCBI

Sequence:

show sequence

TTACTCCCCTGCTGGTGCCTCCCTCCTTGGCGCGCTTCCCACCTGCGATCGGCGCCCTCTTCGC
AGTCACGAACTCGCCAGCAGCTAGCAGCACTGACTAGTAGGAGGGCCCGCCGGAGGAGAGCCGC
GCGGCCCACAGAAGCGGAACGCGCGTCGAGAGCGCCCTGTCCGCTCGCCCCAGACAGATGCCCG
GTTATTCATTACCGCGAGGCCTAGAGGAAAGAGTGGCTGCCGTCTTCCTGCCCACAGCCCGCCG
GACCCTCCGTCGCGGCTGCCCGGTCCCCGGAGCCGCAGCCGCCGAGCCCGGCTGTGCGTGTCGT
GGCTGCTGGGGAGAAAGAGGCTTCCGGAAGCCCCAGAGAGATTGGTGAGGGTGATTTCCCAGGA
AGACGCAGTGTGCTCTGACTTCTGTGACAGTGAGCAACGGGACCAGTGGATGTCCAGATGCTGG
CAATGAGACATGCTCTGGAGTCAGAAGACAGCGAAAAGAGAAGCAGAAGCCCCGGTGGCAAGAG
TCTGAAGCAGGAAGGATGACTGTAGCCTGTGGATTGTACTGCAGTAGGAAACTGTCCTAGCAAG
GCTCCACTTTGCCCCAGCTTCAAGCTGGAAAGGAGGAGAACATGAAACATTGCTTGAAGACAAT
GGCCGAGACAGCAGGTCCCACCCTGCACAGCCACCAGCATCTCTCCCCTCAGCCCTGTCTCCTC
TTCTGCAGTTGGGATCTGCACATTTAAGCCTGAAATTGTCCTGTGAAGTGAAGTATGATCGGAC
AGCCTCTTTTCAGCTTTTATGACAATGGAGACAGAGGAATTGTGGCTCTTGCCAAGGTCACAGG
ATTGGAATACAGAGCCAAGCCACCCCAGGACATGCAAGAGCCTCAGAAGGGAAAAAAGCCCAGC
AGGAAGGGAGAACAAGTAGCCTCTGTCCTGAAGTTGTAACAGCCAGGGGCCAGGATGGAGGAGG
AGGACCCCATAATCTGCCCATCTGGGACTTGGCAGGGGACCTGGGAAAATGTACCCCAACCCAT
CCCTTAAGGGCCTTTGTCTTTGGCCCATTGGCCTAGCATCTACTTCTTCACCGTGTCTGTTCTT
GTCACACCTAGTCAGGTCTGTTTGGGTCTGAGGTGCATGGAACATTCTGGGTAGGCCTCCAGCA
AACGGAAGCTCTTCACCGTGTTTCCAGCCTGGGACCAAGGGCAGCATACTGGCAAAGTTGCCAA
AGCAAGGGACTCCAGCCTCTTAGGAGTTAATGACTCCCTCTCCCCAGCTGTCCTCCCCTTGGTG
CTCCTCTTCCTCCCTCCTCCTGCTCACAGCAGGCAGGGCCTAGACCCGGGAGCCATGCTGCTGT
GCTGTTGCCAGGGGAGCACGGAGGCAGATCTGAGCTATGCAGGGAAAAGGCCCAGCCTGTCAAA
GTGTCTGAGATGAACCGCCGCCGTCCCTGTGCAGCTGGGCTCAGACGTGTCTCAGCTCTTGTTC
TGTGCCTGAGAATGGCGAAACCCAGTGAGGTTCAAGGGCAAACTCGCTATTCATTAGTCAGGGG
TTCTTGACGTCCCGTCTCTCCCAGGGATGAGTTCCCCCCTCCTCTTTCTCCCCCTCCTATGACA
CATTCCTGGGTGCCTTTGGTGAGGACTGCACACCCTCCTCCTGCCTAGCCCCCTCTCCAAAGGC
CCCTGAATAAACTCCCCCCAAGGAGACCAGGCAGGGCAGAGACAATGGCTGCAGGAAATCATTC
AGGCGGGACATGCTGGCCTGCCCTCCACCCAGTCCCCCTGTGGGCCCCACTCCCTTCTGATTCA
GGGCACCCTTGGGCCCCCAGCCTATACAGGCCTGGACAGGAAGAAACCACTGGGAACCACCCTA
AGGACAACATGCTAGTCCAGTGCCATTCTTCGCTGGCTCTGTGGGTGCCTTTGTGGCCTGTACC
GACTGGCTGGCTAATTTTGTGGTTTCTGTACCATCACATGCCTATTTTAAGACACTCTCCAGCA
CTGTCGGTTAGGGAGTGTAAATTTTGCAATATTTTCTGAAATGTGGCAATATCAAAATGTAAAA
GGCACACATACTTGGTCACAAACAAATGGCACTATTTACTCTGTGGGCATATTTGTAAAAGTTG
CCAAAGAATTATATACAAGGATGTTCATCAGAGCATTTCTTTTGAAGAGTAAAGAAATGGACAT
GAACCTGTGGTCCGTTCATACGGTGGAATACCTATGCAGCTGTAAAAATCAGTGTGGTAGATCT
CCGTATATGAGTTGATGTGGAAGGTTGGCCAGTTCACATGATAAGGTGAATAGAATAAGTTACA
GAACAGGCTGTAGAGTATGATCTTATTTGTAGATGTTTAAAACTGAGTCATAAGTATGCTTATA
TACAGATCGTTTCTGGAAGTATGTACTGGAAGTCTACCTCTGGGGAGTGGGGATGGGGGAGTGC
ACTCTTCTATACTGTTATATTTTCTTTTCATGCTCCTAAGGTACTTTTATTGGAAGATGTAAAG
CGGTTCAATGTAATAGGCTTAACTTCTGTCAACTAAGTTGGCGTGGGTGCTTTAAGAGGGTGGT
AGTGATGTTGCTGGAGAAAGTATCCCACAGTCACTGGTGGCTTCAGCCACGGGCCATTTTGGGG
CCTAATAATCACATATCATCATGGTTGCTAGTGTTAATCGAAAACCTACTAAGTGCCAGGCTTA
CTGTCTCTGGGTCTTGCTTACGTGGATGTCATTTTTCCAGTTGCACCAAATCGAAAGAGGTTAA
TTGGTTTGTTGGAGTTCCTTTGTAGGTGAAGGGCAGAGCCAGGAGCTTGGCTAGGGACAGGGGA
GGTGAGTGGGGGATGGTGGATAGGTCTTGGCTCCCAGTTTCCTTCTGGGCAGACATTGCCCCTC
TGCCCTGAGGACCTGCTTGTTTGGGGGAAGAGGCCTTTAGAGGCACCAGGGTCATGCCAGGTGT
TGGACATGGTGAACTGGGAAGTGCTCCCATCTGGCCACAGCGCAGAAGTATCACCGTGCTGGGG
GATGGGGAACAGGGCTGTGAATGGGCCTATTTGCATAAGCAGCATGTGTCTGGAGAGAAAGACA
TCACAGAGCAGAAGAGTGCGGGTGCCCAGGAGTGCACTTGCCACCCCTACTTCATCCCTGAAAG
AGTAAATGGCCTGGAAGGTGTCTCTGAGAGGTAATGCCGCACACCACCCTCCCTGGGGGCAGGG
TCAGGCTACACCTGCCTTAGGTCGGGGGCTGCAGCAGCCTGAGAGCTCTCAGTAGGGCCTCAGT
AGCCTGGGAGGGAGCAGGGGCAGGGGGCAGGGAAAGAGGCGTAATGGGGCTGTCCAGAGGGGCC
TGGGAAACCTGGTCCCTGAGGCCTGGGCACAGCTACAATCACTTCAAATTGGCTGTGGGGCCAG
TGGACTGGGAAGGAAAAAAGCAATAAGAGTGACCAAGTGCAGAAGGCTGTCAGGTCCCAGGTCA
CATGCCTTAGTGCAGTGACTCCTCATCATTTTATGGGGTGTGGGTGTCGTTGGTACACCCATTT
TACAGATGAGGACACCGAGGCCCAGAAAAGTTAAGTTACATGTCCTAAGTCACACAGCTTGTAA
GTGCCAGAACTGAGATCAAAACCAAGTCTCTTTGACTTTAAAGTCTGTACTCTGACCCCAAAGA
GATCCTGTTTGGCCACTTATAGGAGGTCCCTAAAGCTGCAGACTCCCCTTGCCGGCACCCACAT
ATAGAGACATTAACCCTTCCCCTGCAGGGTCACCTCAAATAGTCTTTTAGCTGGGCTTCTCCTG
CAATTCCACCTAATGCCATCCCCTGGGTTTTGCCCAAACCTGAACTGGGCAGTGGGGTGAGAGG
AGGGGTTTACAGGGTTACAGAGCCTCATACAGATAGGAGCCCATGGCTGCTGGTCATCTGCATT
CCTGCAGGATTGGCTGTTCCTTGGGGTCCTTGGCAGGAAAATGAGGATTGCTCCGAGGCCTGCT
CCAGTACTTCCCAGAGGCTGGCCTGGTGTGGGGCTCTGGGAAGGCTGAGGCTGGAGAAGCGTAA
GTAGGAGGGCAGAGATGGCACTCAGGTAGCTTGAATCACCAGGACCCTTCCAAGCCCCACAGGT
TCTGAGGGAGTACTAGGGCCAGCTCTGGGAGAGGTCTCTTCCTATGCTGTGAACCCCCTGCCTT
TCTTGCAGCCTACAACGAATAAATTTTCTTTGCAAAGGAAAAAAAAAAAAAAAAAA

hide sequence

RefSeq Acc Id:

NR_133001

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,361,579 - 89,398,488 (+)	NCBI
CHM1_1	15	89,745,854 - 89,782,728 (+)	NCBI
T2T-CHM13v2.0	15	87,117,636 - 87,154,521 (+)	NCBI

Sequence:

show sequence

GGAGAAACACACACGGGCGGGCGGAGGGGACCCGGGGCGAGTCATCAAGGGCGCGTGGTTCGGC
GTGCCAGGCGCGCTGCTCTGCCTGCTCTCTTGGCTTCTGTCTCCCTTCGACCGATCGCCCCCTA
TCCTGAAGCTTTCCAATGTCATCTTGGAGCCCCAAAGTTTCCTGGGGCCTCCGCGTTGTGCGTC
CCAGAACCCCTTGCCTGCCCCTGAGGGAAACGCGGAGCCATAGGCAGCGGGACGTCGGGAGCCA
GCCCAGGGGAGGCCAGATTCAGCATTTGGACAGCGGCTCTGGGGCGCAGTCGGCCCAGCGAGTT
TGCCGGTGAACAGCCTCGGGCACATGGCGGGTAGGAGGGCCGCAGGGCTGCTCTGGGTCTTGAA
GAAGCAGGACCCAGCCTAGAGGGCATCCCCAGCTCCGAATGGGACACGTTTTCCCGAGATAAAA
GATCCCTTCTGAGCTCACACGGGAGCCCCGGGACCATCCAATCCAGCGTGGATATCCCCAGCCT
AACCAACACCTGTGCTGGGGGGAAAGATAAGACGCCCCCTTTCAGCCAGGAGGTGGACGACCCT
CATGCCCTCAGCTCTCCATTCTTCCCAAAGCAGCTCGGATCCCTAAGTCTGGAGCTGCCAGCGA
GGCTTCCAACCCGCTGCTTGCCATCACCTCCCAGGTCGTTGGTGGCTCCGATTACTCCCCTGCT
GGTGCCTCCCTCCTTGGCGCGCTTCCCACCTGCGATCGGCGCCCTCTTCGCAGTCACGAACTCG
CCAGCAGCTAGCAGCACTGACTAGTAGGAGGGCCCGCCGGAGGAGAGCCGCGCGGCCCACAGAA
GCGGAACGCGCGTCGAGAGCGCCCTGTCCGCTCGCCCCAGACAGATGCCCGGTTATTCATTACC
GCGAGGCCTAGAGGAAAGAGTGGCTGCCGTCTTCCTGCCCACAGCCCGCCGGACCCTCCGTCGC
GGCTGCCCGGTCCCCGGAGCCGCAGCCGCCGAGCCCGGCTGTGCGTGTCGTGGCTGCTGGGGAG
AAAGAGGCTTCCGGACATGCTCTGGAGTCAGAAGACAGCGAAAAGAGAAGCAGAAGCCCCGGTG
GCAAGAGTCTGAAGGAAGGATGACTGTAGCCTGTGGATTGTACTGCAGTAGGAAACTGTCCTAG
CAAGGCTCCACTTTGCCCCAGCTTCAAGCTGGAAAGGAGGAGAACATGAAACATTGCTTGAAGA
CAATGGCCGAGACAGCAGGTCCCACCCTGCACAGCCACCAGCATCTCTCCCCTCAGCCCTGTCT
CCTCTTCTGCAGTTGGGATCTGCACATTTAAGCCTGAAATTGTCCTGTGAAGTGAAGTATGATC
GGACAGCCTCTTTTCAGCTTTTATGACAATGGAGACAGAGGAATTGTGGCTCTTGCCAAGGTCA
CAGGATTGGAATACAGAGCCAAGCCACCCCAGGACATGCAAGAGCCTCAGAAGGGAAAAAAGCC
CAGCAGGAAGGGAGAACAAGTAGCCTCTGTCCTGAAGTTGTAACAGCCAGGGGCCAGGATGGAG
GAGGAGGACCCCATAATCTGCCCATCTGGGACTTGGCAGGGGACCTGGGAAAATGTACCCCAAC
CCATCCCTTAAGGGCCTTTGTCTTTGGCCCATTGGCCTAGCATCTACTTCTTCACCGTGTCTGT
TCTTGTCACACCTAGTCAGGTCTGTTTGGGTCTGAGGTGCATGGAACATTCTGGGTAGGCCTCC
AGCAAACGGAAGCTCTTCACCGTGTTTCCAGCCTGGGACCAAGGGCAGCATACTGGCAAAGTTG
CCAAAGCAAGGGACTCCAGCCTCTTAGGAGTTAATGACTCCCTCTCCCCAGCTGTCCTCCCCTT
GGTGCTCCTCTTCCTCCCTCCTCCTGCTCACAGCAGGCAGGGCCTAGACCCGGGAGCCATGCTG
CTGTGCTGTTGCCAGGGGAGCACGGAGGCAGATCTGAGCTATGCAGGGAAAAGGCCCAGCCTGT
CAAAGTGTCTGAGATGAACCGCCGCCGTCCCTGTGCAGCTGGGCTCAGACGTGTCTCAGCTCTT
GTTCTGTGCCTGAGAATGGCGAAACCCAGTGAGGTTCAAGGGCAAACTCGCTATTCATTAGTCA
GGGGTTCTTGACGTCCCGTCTCTCCCAGGGATGAGTTCCCCCCTCCTCTTTCTCCCCCTCCTAT
GACACATTCCTGGGTGCCTTTGGTGAGGACTGCACACCCTCCTCCTGCCTAGCCCCCTCTCCAA
AGGCCCCTGAATAAACTCCCCCCAAGGAGACCAGGCAGGGCAGAGACAATGGCTGCAGGAAATC
ATTCAGGCGGGACATGCTGGCCTGCCCTCCACCCAGTCCCCCTGTGGGCCCCACTCCCTTCTGA
TTCAGGGCACCCTTGGGCCCCCAGCCTATACAGGCCTGGACAGGAAGAAACCACTGGGAACCAC
CCTAAGGACAACATGCTAGTCCAGTGCCATTCTTCGCTGGCTCTGTGGGTGCCTTTGTGGCCTG
TACCGACTGGCTGGCTAATTTTGTGGTTTCTGTACCATCACATGCCTATTTTAAGACACTCTCC
AGCACTGTCGGTTAGGGAGTGTAAATTTTGCAATATTTTCTGAAATGTGGCAATATCAAAATGT
AAAAGGCACACATACTTGGTCACAAACAAATGGCACTATTTACTCTGTGGGCATATTTGTAAAA
GTTGCCAAAGAATTATATACAAGGATGTTCATCAGAGCATTTCTTTTGAAGAGTAAAGAAATGG
ACATGAACCTGTGGTCCGTTCATACGGTGGAATACCTATGCAGCTGTAAAAATCAGTGTGGTAG
ATCTCCGTATATGAGTTGATGTGGAAGGTTGGCCAGTTCACATGATAAGGTGAATAGAATAAGT
TACAGAACAGGCTGTAGAGTATGATCTTATTTGTAGATGTTTAAAACTGAGTCATAAGTATGCT
TATATACAGATCGTTTCTGGAAGTATGTACTGGAAGTCTACCTCTGGGGAGTGGGGATGGGGGA
GTGCACTCTTCTATACTGTTATATTTTCTTTTCATGCTCCTAAGGTACTTTTATTGGAAGATGT
AAAGCGGTTCAATGTAATAGGCTTAACTTCTGTCAACTAAGTTGGCGTGGGTGCTTTAAGAGGG
TGGTAGTGATGTTGCTGGAGAAAGTATCCCACAGTCACTGGTGGCTTCAGCCACGGGCCATTTT
GGGGCCTAATAATCACATATCATCATGGTTGCTAGTGTTAATCGAAAACCTACTAAGTGCCAGG
CTTACTGTCTCTGGGTCTTGCTTACGTGGATGTCATTTTTCCAGTTGCACCAAATCGAAAGAGG
TTAATTGGTTTGTTGGAGTTCCTTTGTAGGTGAAGGGCAGAGCCAGGAGCTTGGCTAGGGACAG
GGGAGGTGAGTGGGGGATGGTGGATAGGTCTTGGCTCCCAGTTTCCTTCTGGGCAGACATTGCC
CCTCTGCCCTGAGGACCTGCTTGTTTGGGGGAAGAGGCCTTTAGAGGCACCAGGGTCATGCCAG
GTGTTGGACATGGTGAACTGGGAAGTGCTCCCATCTGGCCACAGCGCAGAAGTATCACCGTGCT
GGGGGATGGGGAACAGGGCTGTGAATGGGCCTATTTGCATAAGCAGCATGTGTCTGGAGAGAAA
GACATCACAGAGCAGAAGAGTGCGGGTGCCCAGGAGTGCACTTGCCACCCCTACTTCATCCCTG
AAAGAGTAAATGGCCTGGAAGGTGTCTCTGAGAGGTAATGCCGCACACCACCCTCCCTGGGGGC
AGGGTCAGGCTACACCTGCCTTAGGTCGGGGGCTGCAGCAGCCTGAGAGCTCTCAGTAGGGCCT
CAGTAGCCTGGGAGGGAGCAGGGGCAGGGGGCAGGGAAAGAGGCGTAATGGGGCTGTCCAGAGG
GGCCTGGGAAACCTGGTCCCTGAGGCCTGGGCACAGCTACAATCACTTCAAATTGGCTGTGGGG
CCAGTGGACTGGGAAGGAAAAAAGCAATAAGAGTGACCAAGTGCAGAAGGCTGTCAGGTCCCAG
GTCACATGCCTTAGTGCAGTGACTCCTCATCATTTTATGGGGTGTGGGTGTCGTTGGTACACCC
ATTTTACAGATGAGGACACCGAGGCCCAGAAAAGTTAAGTTACATGTCCTAAGTCACACAGCTT
GTAAGTGCCAGAACTGAGATCAAAACCAAGTCTCTTTGACTTTAAAGTCTGTACTCTGACCCCA
AAGAGATCCTGTTTGGCCACTTATAGGAGGTCCCTAAAGCTGCAGACTCCCCTTGCCGGCACCC
ACATATAGAGACATTAACCCTTCCCCTGCAGGGTCACCTCAAATAGTCTTTTAGCTGGGCTTCT
CCTGCAATTCCACCTAATGCCATCCCCTGGGTTTTGCCCAAACCTGAACTGGGCAGTGGGGTGA
GAGGAGGGGTTTACAGGGTTACAGAGCCTCATACAGATAGGAGCCCATGGCTGCTGGTCATCTG
CATTCCTGCAGGATTGGCTGTTCCTTGGGGTCCTTGGCAGGAAAATGAGGATTGCTCCGAGGCC
TGCTCCAGTACTTCCCAGAGGCTGGCCTGGTGTGGGGCTCTGGGAAGGCTGAGGCTGGAGAAGC
GTAAGTAGGAGGGCAGAGATGGCACTCAGGTAGCTTGAATCACCAGGACCCTTCCAAGCCCCAC
AGGTTCTGAGGGAGTACTAGGGCCAGCTCTGGGAGAGGTCTCTTCCTATGCTGTGAACCCCCTG
CCTTTCTTGCAGCCTACAACGAATAAATTTTCTTTGCAAAGG

hide sequence

RefSeq Acc Id:

NR_133002

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
CHM1_1	15	89,746,796 - 89,782,728 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

Sequence:

show sequence

AGCGGCGCGCGGCCAGGAGCCCCCGCTCCGCCACTGCCGTGCCTGCCTCCCGCAGCTGTCTGCC
ATGCGCTCGCCGGGGCAGGGGCGCCCGGAGGGCGGCTAGAGCTGGGCCTGAGCCCGGGAACGCG
CCTGATCAGGGGTGGCGGAGCCGCGGTCCCCACAGCCGCCCCACCCGCGCCGCTGCCTCGCTGG
GGCCCGGGCCCCCTTCCCGTTACTCCCCTGCTGGTGCCTCCCTCCTTGGCGCGCTTCCCACCTG
CGATCGGCGCCCTCTTCGCAGTCACGAACTCGCCAGCAGCTAGCAGCACTGACTAGTAGGAGGG
CCCGCCGGAGGAGAGGACATGCTCTGGAGTCAGAAGACAGCGAAAAGAGAAGCAGAAGCCCCGG
TGGCAAGAGTCTGAAGCAGGAAGGATGACTGTAGCCTGTGGATTGTACTGCAGTAGGAAACTGT
CCTAGCAAGGCTCCACTTTGCCCCAGCTTCAAGCTGGAAAGGAGGAGAACATGAAACATTGCTT
GAAGACAATGGCCGAGACAGCAGGTCCCACCCTGCACAGCCACCAGCATCTCTCCCCTCAGCCC
TGTCTCCTCTTCTGCAGTTGGGATCTGCACATTTAAGCCTGAAATTGTCCTGTGAAGTGAAGTA
TGATCGGACAGCCTCTTTTCAGCTTTTATGACAATGGAGACAGAGGAATTGTGGCTCTTGCCAA
GGTCACAGGATTGGAATACAGAGCCAAGCCACCCCAGGACATGCAAGAGCCTCAGAAGGGAAAA
AAGCCCAGCAGGAAGGGAGAACAAGTAGCCTCTGTCCTGAAGTTGTAACAGCCAGGGGCCAGGA
TGGAGGAGGAGGACCCCATAATCTGCCCATCTGGGACTTGGCAGGGGACCTGGGAAAATGTACC
CCAACCCATCCCTTAAGGGCCTTTGTCTTTGGCCCATTGGCCTAGCATCTACTTCTTCACCGTG
TCTGTTCTTGTCACACCTAGTCAGGTCTGTTTGGGTCTGAGGTGCATGGAACATTCTGGGTAGG
CCTCCAGCAAACGGAAGCTCTTCACCGTGTTTCCAGCCTGGGACCAAGGGCAGCATACTGGCAA
AGTTGCCAAAGCAAGGGACTCCAGCCTCTTAGGAGTTAATGACTCCCTCTCCCCAGCTGTCCTC
CCCTTGGTGCTCCTCTTCCTCCCTCCTCCTGCTCACAGCAGGCAGGGCCTAGACCCGGGAGCCA
TGCTGCTGTGCTGTTGCCAGGGGAGCACGGAGGCAGATCTGAGCTATGCAGGGAAAAGGCCCAG
CCTGTCAAAGTGTCTGAGATGAACCGCCGCCGTCCCTGTGCAGCTGGGCTCAGACGTGTCTCAG
CTCTTGTTCTGTGCCTGAGAATGGCGAAACCCAGTGAGGTTCAAGGGCAAACTCGCTATTCATT
AGTCAGGGGTTCTTGACGTCCCGTCTCTCCCAGGGATGAGTTCCCCCCTCCTCTTTCTCCCCCT
CCTATGACACATTCCTGGGTGCCTTTGGTGAGGACTGCACACCCTCCTCCTGCCTAGCCCCCTC
TCCAAAGGCCCCTGAATAAACTCCCCCCAAGGAGACCAGGCAGGGCAGAGACAATGGCTGCAGG
AAATCATTCAGGCGGGACATGCTGGCCTGCCCTCCACCCAGTCCCCCTGTGGGCCCCACTCCCT
TCTGATTCAGGGCACCCTTGGGCCCCCAGCCTATACAGGCCTGGACAGGAAGAAACCACTGGGA
ACCACCCTAAGGACAACATGCTAGTCCAGTGCCATTCTTCGCTGGCTCTGTGGGTGCCTTTGTG
GCCTGTACCGACTGGCTGGCTAATTTTGTGGTTTCTGTACCATCACATGCCTATTTTAAGACAC
TCTCCAGCACTGTCGGTTAGGGAGTGTAAATTTTGCAATATTTTCTGAAATGTGGCAATATCAA
AATGTAAAAGGCACACATACTTGGTCACAAACAAATGGCACTATTTACTCTGTGGGCATATTTG
TAAAAGTTGCCAAAGAATTATATACAAGGATGTTCATCAGAGCATTTCTTTTGAAGAGTAAAGA
AATGGACATGAACCTGTGGTCCGTTCATACGGTGGAATACCTATGCAGCTGTAAAAATCAGTGT
GGTAGATCTCCGTATATGAGTTGATGTGGAAGGTTGGCCAGTTCACATGATAAGGTGAATAGAA
TAAGTTACAGAACAGGCTGTAGAGTATGATCTTATTTGTAGATGTTTAAAACTGAGTCATAAGT
ATGCTTATATACAGATCGTTTCTGGAAGTATGTACTGGAAGTCTACCTCTGGGGAGTGGGGATG
GGGGAGTGCACTCTTCTATACTGTTATATTTTCTTTTCATGCTCCTAAGGTACTTTTATTGGAA
GATGTAAAGCGGTTCAATGTAATAGGCTTAACTTCTGTCAACTAAGTTGGCGTGGGTGCTTTAA
GAGGGTGGTAGTGATGTTGCTGGAGAAAGTATCCCACAGTCACTGGTGGCTTCAGCCACGGGCC
ATTTTGGGGCCTAATAATCACATATCATCATGGTTGCTAGTGTTAATCGAAAACCTACTAAGTG
CCAGGCTTACTGTCTCTGGGTCTTGCTTACGTGGATGTCATTTTTCCAGTTGCACCAAATCGAA
AGAGGTTAATTGGTTTGTTGGAGTTCCTTTGTAGGTGAAGGGCAGAGCCAGGAGCTTGGCTAGG
GACAGGGGAGGTGAGTGGGGGATGGTGGATAGGTCTTGGCTCCCAGTTTCCTTCTGGGCAGACA
TTGCCCCTCTGCCCTGAGGACCTGCTTGTTTGGGGGAAGAGGCCTTTAGAGGCACCAGGGTCAT
GCCAGGTGTTGGACATGGTGAACTGGGAAGTGCTCCCATCTGGCCACAGCGCAGAAGTATCACC
GTGCTGGGGGATGGGGAACAGGGCTGTGAATGGGCCTATTTGCATAAGCAGCATGTGTCTGGAG
AGAAAGACATCACAGAGCAGAAGAGTGCGGGTGCCCAGGAGTGCACTTGCCACCCCTACTTCAT
CCCTGAAAGAGTAAATGGCCTGGAAGGTGTCTCTGAGAGGTAATGCCGCACACCACCCTCCCTG
GGGGCAGGGTCAGGCTACACCTGCCTTAGGTCGGGGGCTGCAGCAGCCTGAGAGCTCTCAGTAG
GGCCTCAGTAGCCTGGGAGGGAGCAGGGGCAGGGGGCAGGGAAAGAGGCGTAATGGGGCTGTCC
AGAGGGGCCTGGGAAACCTGGTCCCTGAGGCCTGGGCACAGCTACAATCACTTCAAATTGGCTG
TGGGGCCAGTGGACTGGGAAGGAAAAAAGCAATAAGAGTGACCAAGTGCAGAAGGCTGTCAGGT
CCCAGGTCACATGCCTTAGTGCAGTGACTCCTCATCATTTTATGGGGTGTGGGTGTCGTTGGTA
CACCCATTTTACAGATGAGGACACCGAGGCCCAGAAAAGTTAAGTTACATGTCCTAAGTCACAC
AGCTTGTAAGTGCCAGAACTGAGATCAAAACCAAGTCTCTTTGACTTTAAAGTCTGTACTCTGA
CCCCAAAGAGATCCTGTTTGGCCACTTATAGGAGGTCCCTAAAGCTGCAGACTCCCCTTGCCGG
CACCCACATATAGAGACATTAACCCTTCCCCTGCAGGGTCACCTCAAATAGTCTTTTAGCTGGG
CTTCTCCTGCAATTCCACCTAATGCCATCCCCTGGGTTTTGCCCAAACCTGAACTGGGCAGTGG
GGTGAGAGGAGGGGTTTACAGGGTTACAGAGCCTCATACAGATAGGAGCCCATGGCTGCTGGTC
ATCTGCATTCCTGCAGGATTGGCTGTTCCTTGGGGTCCTTGGCAGGAAAATGAGGATTGCTCCG
AGGCCTGCTCCAGTACTTCCCAGAGGCTGGCCTGGTGTGGGGCTCTGGGAAGGCTGAGGCTGGA
GAAGCGTAAGTAGGAGGGCAGAGATGGCACTCAGGTAGCTTGAATCACCAGGACCCTTCCAAGC
CCCACAGGTTCTGAGGGAGTACTAGGGCCAGCTCTGGGAGAGGTCTCTTCCTATGCTGTGAACC
CCCTGCCTTTCTTGCAGCCTACAACGAATAAATTTTCTTTGCAAAGG

hide sequence

RefSeq Acc Id:

NR_133003

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
CHM1_1	15	89,752,374 - 89,782,728 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

Sequence:

show sequence

GATTCTCACAACTTCTGCGTGCGAGCGCCCGCCCCACCGACCGCCCCGGCCCGGCCCGCAAGAG
CCAGAGGAGCCGAGAGGAGCCCAGCGCCGGCCCAGCGGACTCCAGCTCGACGGAGCGGCCGCGC
CCCGACCAGTTACTCCCCTGCTGGTGCCTCCCTCCTTGGCGCGCTTCCCACCTGCGATCGGCGC
CCTCTTCGCAGTCACGAACTCGCCAGCAGCTAGCAGCACTGACTAGTAGGAGGGCCCGCCGGAG
GAGAGGAAGCCCCAGAGAGATTGGTGAGGGTGATTTCCCAGGAAGACGCAGTGTGCTCTGACTT
CTGTGACAGTGAGCAACGGGACCAGTGGATGTCCAGATGCTGGCAATGAGACATGCTCTGGAGT
CAGAAGACAGCGAAAAGAGAAGCAGAAGCCCCGGTGGCAAGAGTCTGAAGCAGGAAGGATGACT
GTAGCCTGTGGATTGTACTGCAGTAGGAAACTGTCCTAGCAAGGCTCCACTTTGCCCCAGCTTC
AAGCTGGAAAGGAGGAGAACATGAAACATTGCTTGAAGACAATGGCCGAGACAGCAGGTCCCAC
CCTGCACAGCCACCAGCATCTCTCCCCTCAGCCCTGTCTCCTCTTCTGCAGTTGGGATCTGCAC
ATTTAAGCCTGAAATTGTCCTGTGAAGTGAAGTATGATCGGACAGCCTCTTTTCAGCTTTTATG
ACAATGGAGACAGAGGAATTGTGGCTCTTGCCAAGGTCACAGGATTGGAATACAGAGCCAAGCC
ACCCCAGGACATGCAAGAGCCTCAGAAGGGAAAAAAGCCCAGCAGGAAGGGAGAACAAGTAGCC
TCTGTCCTGAAGTTGTAACAGCCAGGGGCCAGGATGGAGGAGGAGGACCCCATAATCTGCCCAT
CTGGGACTTGGCAGGGGACCTGGGAAAATGTACCCCAACCCATCCCTTAAGGGCCTTTGTCTTT
GGCCCATTGGCCTAGCATCTACTTCTTCACCGTGTCTGTTCTTGTCACACCTAGTCAGGTCTGT
TTGGGTCTGAGGTGCATGGAACATTCTGGGTAGGCCTCCAGCAAACGGAAGCTCTTCACCGTGT
TTCCAGCCTGGGACCAAGGGCAGCATACTGGCAAAGTTGCCAAAGCAAGGGACTCCAGCCTCTT
AGGAGTTAATGACTCCCTCTCCCCAGCTGTCCTCCCCTTGGTGCTCCTCTTCCTCCCTCCTCCT
GCTCACAGCAGGCAGGGCCTAGACCCGGGAGCCATGCTGCTGTGCTGTTGCCAGGGGAGCACGG
AGGCAGATCTGAGCTATGCAGGGAAAAGGCCCAGCCTGTCAAAGTGTCTGAGATGAACCGCCGC
CGTCCCTGTGCAGCTGGGCTCAGACGTGTCTCAGCTCTTGTTCTGTGCCTGAGAATGGCGAAAC
CCAGTGAGGTTCAAGGGCAAACTCGCTATTCATTAGTCAGGGGTTCTTGACGTCCCGTCTCTCC
CAGGGATGAGTTCCCCCCTCCTCTTTCTCCCCCTCCTATGACACATTCCTGGGTGCCTTTGGTG
AGGACTGCACACCCTCCTCCTGCCTAGCCCCCTCTCCAAAGGCCCCTGAATAAACTCCCCCCAA
GGAGACCAGGCAGGGCAGAGACAATGGCTGCAGGAAATCATTCAGGCGGGACATGCTGGCCTGC
CCTCCACCCAGTCCCCCTGTGGGCCCCACTCCCTTCTGATTCAGGGCACCCTTGGGCCCCCAGC
CTATACAGGCCTGGACAGGAAGAAACCACTGGGAACCACCCTAAGGACAACATGCTAGTCCAGT
GCCATTCTTCGCTGGCTCTGTGGGTGCCTTTGTGGCCTGTACCGACTGGCTGGCTAATTTTGTG
GTTTCTGTACCATCACATGCCTATTTTAAGACACTCTCCAGCACTGTCGGTTAGGGAGTGTAAA
TTTTGCAATATTTTCTGAAATGTGGCAATATCAAAATGTAAAAGGCACACATACTTGGTCACAA
ACAAATGGCACTATTTACTCTGTGGGCATATTTGTAAAAGTTGCCAAAGAATTATATACAAGGA
TGTTCATCAGAGCATTTCTTTTGAAGAGTAAAGAAATGGACATGAACCTGTGGTCCGTTCATAC
GGTGGAATACCTATGCAGCTGTAAAAATCAGTGTGGTAGATCTCCGTATATGAGTTGATGTGGA
AGGTTGGCCAGTTCACATGATAAGGTGAATAGAATAAGTTACAGAACAGGCTGTAGAGTATGAT
CTTATTTGTAGATGTTTAAAACTGAGTCATAAGTATGCTTATATACAGATCGTTTCTGGAAGTA
TGTACTGGAAGTCTACCTCTGGGGAGTGGGGATGGGGGAGTGCACTCTTCTATACTGTTATATT
TTCTTTTCATGCTCCTAAGGTACTTTTATTGGAAGATGTAAAGCGGTTCAATGTAATAGGCTTA
ACTTCTGTCAACTAAGTTGGCGTGGGTGCTTTAAGAGGGTGGTAGTGATGTTGCTGGAGAAAGT
ATCCCACAGTCACTGGTGGCTTCAGCCACGGGCCATTTTGGGGCCTAATAATCACATATCATCA
TGGTTGCTAGTGTTAATCGAAAACCTACTAAGTGCCAGGCTTACTGTCTCTGGGTCTTGCTTAC
GTGGATGTCATTTTTCCAGTTGCACCAAATCGAAAGAGGTTAATTGGTTTGTTGGAGTTCCTTT
GTAGGTGAAGGGCAGAGCCAGGAGCTTGGCTAGGGACAGGGGAGGTGAGTGGGGGATGGTGGAT
AGGTCTTGGCTCCCAGTTTCCTTCTGGGCAGACATTGCCCCTCTGCCCTGAGGACCTGCTTGTT
TGGGGGAAGAGGCCTTTAGAGGCACCAGGGTCATGCCAGGTGTTGGACATGGTGAACTGGGAAG
TGCTCCCATCTGGCCACAGCGCAGAAGTATCACCGTGCTGGGGGATGGGGAACAGGGCTGTGAA
TGGGCCTATTTGCATAAGCAGCATGTGTCTGGAGAGAAAGACATCACAGAGCAGAAGAGTGCGG
GTGCCCAGGAGTGCACTTGCCACCCCTACTTCATCCCTGAAAGAGTAAATGGCCTGGAAGGTGT
CTCTGAGAGGTAATGCCGCACACCACCCTCCCTGGGGGCAGGGTCAGGCTACACCTGCCTTAGG
TCGGGGGCTGCAGCAGCCTGAGAGCTCTCAGTAGGGCCTCAGTAGCCTGGGAGGGAGCAGGGGC
AGGGGGCAGGGAAAGAGGCGTAATGGGGCTGTCCAGAGGGGCCTGGGAAACCTGGTCCCTGAGG
CCTGGGCACAGCTACAATCACTTCAAATTGGCTGTGGGGCCAGTGGACTGGGAAGGAAAAAAGC
AATAAGAGTGACCAAGTGCAGAAGGCTGTCAGGTCCCAGGTCACATGCCTTAGTGCAGTGACTC
CTCATCATTTTATGGGGTGTGGGTGTCGTTGGTACACCCATTTTACAGATGAGGACACCGAGGC
CCAGAAAAGTTAAGTTACATGTCCTAAGTCACACAGCTTGTAAGTGCCAGAACTGAGATCAAAA
CCAAGTCTCTTTGACTTTAAAGTCTGTACTCTGACCCCAAAGAGATCCTGTTTGGCCACTTATA
GGAGGTCCCTAAAGCTGCAGACTCCCCTTGCCGGCACCCACATATAGAGACATTAACCCTTCCC
CTGCAGGGTCACCTCAAATAGTCTTTTAGCTGGGCTTCTCCTGCAATTCCACCTAATGCCATCC
CCTGGGTTTTGCCCAAACCTGAACTGGGCAGTGGGGTGAGAGGAGGGGTTTACAGGGTTACAGA
GCCTCATACAGATAGGAGCCCATGGCTGCTGGTCATCTGCATTCCTGCAGGATTGGCTGTTCCT
TGGGGTCCTTGGCAGGAAAATGAGGATTGCTCCGAGGCCTGCTCCAGTACTTCCCAGAGGCTGG
CCTGGTGTGGGGCTCTGGGAAGGCTGAGGCTGGAGAAGCGTAAGTAGGAGGGCAGAGATGGCAC
TCAGGTAGCTTGAATCACCAGGACCCTTCCAAGCCCCACAGGTTCTGAGGGAGTACTAGGGCCA
GCTCTGGGAGAGGTCTCTTCCTATGCTGTGAACCCCCTGCCTTTCTTGCAGCCTACAACGAATA
AATTTTCTTTGCAAAGG

hide sequence

RefSeq Acc Id:

NR_190290

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,104 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,134,136 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190291

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,104 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,134,136 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190292

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,104 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,134,136 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190293

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,104 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,134,136 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190294

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,104 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,134,136 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190295

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,104 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,134,136 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190296

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,104 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,134,136 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190297

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,104 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,134,136 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190298

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190299

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190300

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190301

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190302

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190303

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190304

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190305

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190306

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190307

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190308

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190309

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,379,119 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,135,151 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190310

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,361,579 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,117,636 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190311

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190312

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190313

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190314

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190315

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190316

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190317

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190318

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190319

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190320

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190321

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190322

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190323

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190324

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190325

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

RefSeq Acc Id:

NR_190326

RefSeq Status:

VALIDATED

Type:

NON-CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,398,488 (+)	NCBI
T2T-CHM13v2.0	15	87,118,566 - 87,154,521 (+)	NCBI

Promoters

RGD ID:

15096932

Promoter ID:

EPDNEWNC_H1762

Type:

initiation region

Name:

MIR9-3HG_1

Description:

MIR9-3 host gene [Source:HGNC Symbol;Acc:HGNC:27388]

SO ACC ID:

SO:0000170

Source:

EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,362,509 - 89,362,569	EPDNEWNC

RGD ID:

15096928

Promoter ID:

EPDNEWNC_H1763

Type:

initiation region

Name:

MIR9-3HG_2

Description:

MIR9-3 host gene [Source:HGNC Symbol;Acc:HGNC:27388]

SO ACC ID:

SO:0000170

Source:

EPDNEWNC (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Experiment Methods:

Single-end sequencing.; Paired-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	15	89,378,097 - 89,378,157	EPDNEWNC

Additional Information

External Database Links

Database	Acc Id	Source(s)
COSMIC	MIR9-3HG	COSMIC
Ensembl Genes	ENSG00000255571	Ensembl, ENTREZGENE
Ensembl Transcript	ENST00000536780	ENTREZGENE
	ENST00000654079	ENTREZGENE
	ENST00000654171	ENTREZGENE
	ENST00000654184	ENTREZGENE
	ENST00000657897	ENTREZGENE
	ENST00000658764	ENTREZGENE
	ENST00000658770	ENTREZGENE
	ENST00000659235	ENTREZGENE
	ENST00000661036	ENTREZGENE
	ENST00000661040	ENTREZGENE
	ENST00000666816	ENTREZGENE
	ENST00000669499	ENTREZGENE
	ENST00000670779	ENTREZGENE
GTEx	ENSG00000255571	GTEx
HGNC ID	HGNC:27388	ENTREZGENE
Human Proteome Map	MIR9-3HG	Human Proteome Map
NCBI Gene	LINC00925	ENTREZGENE
RNAcentral	URS00001BFDB8	RNACentral
	URS00002D5277	RNACentral
	URS00005806C9	RNACentral
	URS000061ACC1	RNACentral
	URS000075DAA9	RNACentral
	URS00007672C0	RNACentral
	URS00008BB927	RNACentral
	URS00008E3959	RNACentral
	URS0000EEB215	RNACentral
	URS0000EEBBB4	RNACentral
	URS0000EEBFFD	RNACentral
	URS0000EEC3C2	RNACentral
	URS0000EEC6EB	RNACentral
	URS0000EED486	RNACentral
	URS0000EED78C	RNACentral
	URS0000EED7DE	RNACentral
	URS0000EED8CC	RNACentral
	URS0000EEDDBC	RNACentral
	URS0000EEE28C	RNACentral
	URS0000EEE443	RNACentral
	URS0000EEEA36	RNACentral
	URS0000EEF436	RNACentral
	URS0000EEFA3A	RNACentral
	URS0000EEFB9F	RNACentral
	URS0000EF000B	RNACentral
	URS0000EF1123	RNACentral
	URS0000EF13E2	RNACentral
	URS0000EF1591	RNACentral
	URS0000EF1C0E	RNACentral
	URS0000EF1D1C	RNACentral
	URS0000EF2497	RNACentral
	URS0000EF26B1	RNACentral
	URS0000EF26B9	RNACentral
	URS0000EF28E3	RNACentral
	URS0000EF2E83	RNACentral
	URS0000EF3666	RNACentral
	URS0000EF3B2D	RNACentral
	URS0000EF3E3C	RNACentral
	URS0000EF3F32	RNACentral
	URS0000EF40E3	RNACentral
	URS0000EF4400	RNACentral
	URS0000EF4411	RNACentral
	URS0000EF4C77	RNACentral
	URS0000EF4E01	RNACentral
	URS0000EF55E1	RNACentral
	URS0000EF55ED	RNACentral
	URS0000EF57F8	RNACentral
	URS0000EF5B38	RNACentral
	URS0000EF5D82	RNACentral
	URS0000EF5F31	RNACentral
	URS0000EF62C7	RNACentral
	URS0000EF6370	RNACentral
	URS0000EF64D2	RNACentral
	URS0000EF6B7D	RNACentral
	URS0000EF6BE7	RNACentral
	URS0000EF722C	RNACentral
	URS00025F3D73	RNACentral

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2015-10-20	MIR9-3HG	MIR9-3 host gene	LINC00925	long intergenic non-protein coding RNA 925	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

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