chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183923501339235014GA26GENIChomozygous140302683
183923528539235286A8GENIChomozygous140219641
183924195239241953TC34GENIChomozygous140302684
183924265139242651T27GENIChomozygous140219642
183924704839247048G22GENICpossibly homozygous140219643
183924827539248281AAAAAG17GENIChomozygous140219644
183925046039250461AG27GENIChomozygous140302685
183925087739250885CCAAAAGT25GENIChomozygous140219645
183925099439250995AC18GENIChomozygous140302686
183925189739251898CT15GENIChomozygous140302687
183925236139252362AG17GENIChomozygous140302688
183925277839252778AAATA29GENIChomozygous140219646
183925533939255339AC23GENIChomozygous140219647
183925662439256625GA30GENIChomozygous140302689
183925679339256794CT24GENIChomozygous140302690