chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161263024161263025GT47GENIChomozygous793431130
3161263208161263209TC49GENIChomozygous793431131
3161264132161264133AG46GENIChomozygous793431132
3161264323161264324GA43GENICpossibly homozygous793431133
3161265050161265051CA11GENIChomozygous793431134
3161266300161266301GT23GENIChomozygous793431135
3161269826161269827GA48GENIChomozygous793431136
3161270225161270226TC47GENIChomozygous793431137