chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102955936729559368GA64GENIChomozygous68349018
102955944829559449TC64GENIChomozygous67835641
102955956229559563AG34GENIChomozygous67835645
102956035029560351GA34GENIChomozygous68349020
102956089429560895CT46GENICpossibly homozygous67835657
102956095329560954CT65GENICpossibly homozygous67835665
102956095829560959AG66GENICpossibly homozygous67835668
102956183829561839CT39GENIChomozygous68349022
102956195629561957TA66GENIChomozygous68349024
102956218729562188AG49GENIChomozygous67835686
102956222429562225AT46GENIChomozygous68349026
102956254829562549TG56GENIChomozygous68349029
102956255829562559CT60GENIChomozygous68349031
102956302629563027GA32GENIChomozygous68349033
102956305429563055TG31GENIChomozygous67835704
102956332629563327TG50GENICheterozygous68349035
102956339829563399TC54GENICpossibly homozygous67835708
102956341629563417CT52GENIChomozygous68349037
102956367529563676AG44GENIChomozygous67835713
102956368329563684GA40GENIChomozygous68349039
102956400329564004GA25GENICpossibly homozygous68349041
102956410029564101CT35GENICpossibly homozygous68349043
102956469929564700CT51GENIChomozygous68349045
102956548429565485CT67GENIChomozygous68349047
102956639529566396GA53GENIChomozygous67835729
102956664829566649GT68GENIChomozygous67835733
102956719729567198AG44GENIChomozygous67835737
102956748929567490AG26GENICheterozygous68349049
102956760229567603CT46GENIChomozygous67835745
102956768229567683TC48GENIChomozygous67835749
102956810629568107GA36GENIChomozygous67835754
102956814129568142GC38GENIChomozygous67835758