chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X17571481757149GA35GENIChomozygous108216186
X17606221760623GA33GENIChomozygous108216188
X17624221762423CT38GENIChomozygous108216190
X17651191765120GA37GENICpossibly homozygous108216192
X17675531767554CT44GENIChomozygous108216194
X17720021772003AC42GENIChomozygous108216196
X17770891777090AT53GENIChomozygous108216198
X17808251780826AG47GENIChomozygous108216200
X17855801785581CG34GENIChomozygous119899454
X17765851776586TG26GENICheterozygous119899452
X17835571783558AG26GENICpossibly homozygous119899453
X17786621778663AT53GENIChomozygous108437108
X17858471785848GA32GENIChomozygous119899455
X17866081786609TG21GENIChomozygous108216202
X17869671786968CT29GENIChomozygous108216204