chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X17571481757149GA14GENIChomozygous108216186
X17606221760623GA45GENIChomozygous108216188
X17624221762423CT14GENIChomozygous108216190
X17651191765120GA24GENIChomozygous108216192
X17675531767554CT28GENIChomozygous108216194
X17720021772003AC10GENICpossibly homozygous108216196
X17770891777090AT16GENIChomozygous108216198
X17808251780826AG13GENIChomozygous108216200
X17866081786609TG18GENICpossibly homozygous108216202
X17869671786968CT21GENIChomozygous108216204