chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3161263024161263025GT50GENIChomozygous779727229
3161263208161263209TC49GENIChomozygous779727230
3161264132161264133AG34GENIChomozygous779727231
3161264323161264324GA53GENIChomozygous779727232
3161265050161265051CA9GENICpossibly homozygous779727233
3161269826161269827GA85GENIChomozygous779727234
3161270225161270226TC38GENIChomozygous779727235