chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1753054355305436GC39GENIChomozygous782661477
1753054505305451AG39GENIChomozygous782661478
1753056815305682GA46GENIChomozygous782661479
1753059855305986CT29GENIChomozygous782661480
1753086605308661GA20GENIChomozygous782661481
1753089325308933CT73GENIChomozygous782661482
1753091255309126CG48GENICpossibly homozygous782661483
1753093335309334CT54GENIChomozygous782661484
1753094665309467GA60GENIChomozygous782661485
1753096275309628TC56GENIChomozygous782661486
1753101255310126AG52GENICpossibly homozygous782661487
1753101975310198TA60GENIChomozygous782661488
1753104855310486AG43GENICpossibly homozygous782661489
1753105045310505AG46GENICpossibly homozygous782661490