chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X17571481757149GA15GENIChomozygous108216186
X17606221760623GA24GENIChomozygous108216188
X17651191765120GA19GENIChomozygous108216192
X17675531767554CT15GENIChomozygous108216194
X17720021772003AC11GENIChomozygous108216196
X17770891777090AT9GENIChomozygous108216198
X17808251780826AG14GENIChomozygous108216200
X17866081786609TG8GENICpossibly homozygous108216202
X17869671786968CT22GENIChomozygous108216204