chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5154644362154644363GT7GENICheterozygous118913638
5154644847154644848TC32GENIChomozygous114062048
5154645070154645071TC21GENIChomozygous114062050
5154645537154645538CG7GENIChomozygous114062052
5154645604154645605TA12GENIChomozygous114062054
5154645798154645799TG10GENIChomozygous114062056
5154645807154645808CA15GENIChomozygous114062058
5154647513154647514CT19GENIChomozygous114062062
5154647595154647596GT18GENIChomozygous114062064
5154648061154648062AG35GENIChomozygous114062066
5154648534154648535CT25GENIChomozygous114062068
5154649515154649516TC29GENIChomozygous114062080
5154649729154649730CT23GENIChomozygous114062082
5154650200154650201GA21GENIChomozygous114062084
5154650505154650506GA19GENIChomozygous114062086
5154650938154650939GA16GENIChomozygous114062088
5154651475154651476GC10GENIChomozygous114062090
5154652202154652203AC26GENIChomozygous114062091