chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183923501339235014GA70GENIChomozygous140302683
183923528539235286A52GENIChomozygous140219641
183924195239241953TC66GENIChomozygous140302684
183924265139242651T47GENICpossibly homozygous140219642
183924704839247048G48GENICpossibly homozygous140219643
183924827539248281AAAAAG51GENIChomozygous140219644
183925046039250461AG41GENIChomozygous140302685
183925087739250885CCAAAAGT46GENIChomozygous140219645
183925099439250995AC50GENIChomozygous140302686
183925189739251898CT13GENIChomozygous140302687
183925236139252362AG44GENIChomozygous140302688
183925277839252778AAATA44GENIChomozygous140219646
183925533939255339AC54GENICpossibly homozygous140219647
183925662439256625GA54GENIChomozygous140302689
183925679339256794CT50GENIChomozygous140302690
183924304939243059GAGAGAGAGT31GENICheterozygous140926308
183925193139251931AAGAGCACTGATTGCTCTTCCGGAGGTCCTG8GENICheterozygous147884041