chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1205523234205523235TG24GENIChomozygous141295795
1205523458205523459G22GENIChomozygous403972922
1205523458205523459GC22GENICheterozygous403972923
1205523460205523461GC22GENIChomozygous141295796
1205523462205523463GC21GENIChomozygous141295797
1205524726205524727AC13GENIChomozygous141295798
1205524848205524849GA18GENIChomozygous141295799
1205524894205524895AT16GENIChomozygous141295800
1205526272205526273AG14GENIChomozygous141295801
1205527203205527204CT23GENIChomozygous141295802
1205527432205527433CT21GENIChomozygous141295803
1205529174205529175CA13GENIChomozygous141295804
1205529500205529501TC13GENIChomozygous141295805
1205529986205529987GA23GENICpossibly homozygous141295806
1205530001205530002AG25GENICpossibly homozygous141295807
1205530388205530389TC25GENICpossibly homozygous141295808
1205530920205530921AG19GENIChomozygous141295809
1205531090205531091GT15GENIChomozygous141295810