chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160016603160016604AG12GENIChomozygous886363945
5160017047160017048AG17GENIChomozygous886363946
5160018775160018776AG15GENIChomozygous886363947
5160020946160020947AG9GENIChomozygous886363948
5160021044160021045CT8GENIChomozygous886363949
5160021100160021101GA14GENIChomozygous886363950
5160028386160028387CT11GENIChomozygous886363951
5160030069160030070GA18GENIChomozygous886363952
5160030614160030615CT3GENICheterozygous886363953
5160031340160031341AG8GENICheterozygous886363954
5160034484160034485CT10GENIChomozygous886363955
5160035171160035172TC13GENIChomozygous886363956
5160035383160035384GA9GENIChomozygous886363957
5160035866160035867CT7GENICheterozygous886363958
5160039618160039619AG15GENIChomozygous886363959
5160039756160039757AG9GENIChomozygous886363960
5160039838160039839GA18GENIChomozygous886363961
5160039869160039870CT13GENIChomozygous886363962
5160041778160041779CT18GENIChomozygous886363963
5160042955160042956AG7GENIChomozygous886363964
5160046459160046460GT24GENIChomozygous886363965
5160046496160046497TG20GENIChomozygous886363966
5160046573160046574TG12GENIChomozygous886363967
5160049547160049548TC10GENIChomozygous886363968
5160050237160050238GA28GENIChomozygous886363969
5160051630160051631GT11GENIChomozygous886363970
5160051711160051712TC14GENIChomozygous886363971
5160051767160051768AG18GENIChomozygous886363972
5160052057160052058CT23GENIChomozygous886363973
5160053029160053030TC20GENICpossibly homozygous886363974
5160053483160053484GA9GENIChomozygous886363975
5160053965160053966AG17GENIChomozygous886363976
5160056525160056526GA13GENIChomozygous886363977
5160057102160057103GA14GENIChomozygous886363978
5160057112160057113TC10GENIChomozygous886363979
5160057232160057233TG23GENIChomozygous886363980
5160059208160059209CT22GENIChomozygous886363981
5160059871160059872AG15GENICheterozygous886363982
5160068937160068938TA9GENICheterozygous886363983