chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1420710752071076AG50GENIChomozygous113316810
1420725732072574CT49GENICpossibly homozygous113640087
1420729872072988CT45GENICpossibly homozygous113640089
1420739372073938AG52GENIChomozygous113640091
1420740852074086TC53GENIChomozygous113316813
1420753442075345AG46GENIChomozygous113316815
1420757802075781AG49GENIChomozygous113640093
1420764512076452CT44GENIChomozygous113845897
1420772752077276GC61GENIChomozygous113640095
1420779052077906CT32GENIChomozygous113640097
1420782692078270GA46GENIChomozygous113316820
1420785932078594AG46GENIChomozygous113316821
1420786672078668CT42GENIChomozygous113316822
1420788472078848CT41GENIChomozygous113640099
1420788552078856AG42GENIChomozygous113640101
1420792942079295CT44GENIChomozygous113640103
1420794792079480CT43GENIChomozygous113640105
1420797232079724GA53GENIChomozygous113640107
1420805142080515GA49GENIChomozygous113640109
1420815242081525GA47GENIChomozygous113640111
1420830902083091AG52GENIChomozygous113316827
1420774872077487T40GENIChomozygous129116451
1420833022083303A55GENIChomozygous129116452
1420779052077905A32GENIChomozygous132178879