chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5154644847154644848TC30GENIChomozygous114062048
5154645070154645071TC20GENIChomozygous114062050
5154645537154645538CG22GENIChomozygous114062052
5154645604154645605TA25GENIChomozygous114062054
5154645798154645799TG27GENIChomozygous114062056
5154645807154645808CA27GENIChomozygous114062058
5154647513154647514CT23GENIChomozygous114062062
5154647595154647596GT21GENIChomozygous114062064
5154648061154648062AG25GENIChomozygous114062066
5154648534154648535CT21GENIChomozygous114062068
5154649515154649516TC17GENIChomozygous114062080
5154649729154649730CT25GENIChomozygous114062082
5154650200154650201GA12GENIChomozygous114062084
5154650505154650506GA32GENIChomozygous114062086
5154650938154650939GA31GENIChomozygous114062088
5154651475154651476GC22GENIChomozygous114062090
5154652202154652203AC28GENIChomozygous114062091