chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
826847492684750T-6GENIChomozygous695863593
826847642684765G-6GENIChomozygous695863594
826848372684838GGA4GENIChomozygous695863595
826848982684899TA8GENIChomozygous537016837
826849112684912GA10GENIChomozygous537016838
826863492686350T-39GENICheterozygous695863596
826916102691611C-17GENIChomozygous695863597
826918612691862AAT11GENIChomozygous695863598
826921142692115GT79GENICheterozygous537016839
826921572692158CG76GENICheterozygous534667090
826921772692178AC77GENICheterozygous537016840
826922192692220TA89GENICheterozygous537016841
826922312692232T-63GENICheterozygous695863599
826922412692242CG82GENICheterozygous537016842
826922802692281CA76GENICheterozygous537016843
826932452693246AT70GENICheterozygous537016844
826932522693253GA73GENICheterozygous537016845
826936392693640GT15GENICpossibly homozygous534667091
826936672693668GT13GENICheterozygous537016846
826936692693670GT13GENICheterozygous537016847
826962842696285AT23GENIChomozygous537016848
826963602696361CT13GENIChomozygous537016849
827001022700103GGA12GENIChomozygous695863600
827001142700115AAC12GENIChomozygous695863601
827002772700278CCT15GENIChomozygous695863602
827002822700283T-13GENIChomozygous695863603