chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1112278100112278101TC47GENIChomozygous778528809
1112278621112278622AC45GENICpossibly homozygous778528810
1112278818112278819CT60GENIChomozygous778528811
1112279010112279011AG62GENIChomozygous778528812