chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
31249163212491633AG36GENIChomozygous111449988
31249179912491800CT16GENIChomozygous119967433
31249269112492692CA19GENIChomozygous111449989
31249329912493300GA16GENIChomozygous119967434
31249492512494926GA21GENIChomozygous119967435
31249548312495484CA17GENIChomozygous119667067
31249760112497602AG24GENIChomozygous111449995
31249791012497911GA34GENIChomozygous111449996
31250156112501562CT11GENIChomozygous111449999
31250202812502029CT18GENIChomozygous119967436
31250270012502701TC32GENIChomozygous119772875
31250383312503834TC24GENICpossibly homozygous111450000
31250497212504973AG8GENIChomozygous111450001
31250569512505696TC17GENIChomozygous111450002
31250632812506329CA18GENIChomozygous111450003
31250656312506564GC20GENIChomozygous111450005
31250660512506606GA17GENIChomozygous119967437
31250668612506687GT25GENIChomozygous111450006
31250684512506846TA27GENIChomozygous111450007
31250686412506865GT25GENIChomozygous111450008
31250810812508109TA17GENIChomozygous111450011
31250828212508283AC14GENIChomozygous119967438
31250837712508378AC11GENIChomozygous111450012
31250897512508976GA4GENIChomozygous119967439