chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216953015216953016CT53GENICpossibly homozygous120512023
1216953037216953038GA51GENICpossibly homozygous120512024
1216953189216953190AG46GENIChomozygous120512025
1216953616216953617GA64GENIChomozygous120512026
1216953819216953820AG47GENIChomozygous108536250
1216954387216954388TC57GENIChomozygous108536255
1216954977216954978AC59GENIChomozygous125408758
1216953852216953853GA53GENIChomozygous132008462
1216953888216953889CT54GENIChomozygous132008463
1216954206216954207GA58GENIChomozygous132008464
1216955561216955562TC59GENIChomozygous132008465
1216954399216954402ATT56GENIChomozygous131992149
1216954405216954405C58GENIChomozygous131992150
1216954406216954406GC57GENIChomozygous131992151