chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109727756109727757GA45GENIChomozygous51599659
10109730194109730196TT--24GENICheterozygous51599660
10109730195109730196T-24GENICheterozygous51599661
10109730311109730312TTTTTTG27GENIChomozygous51599662
10109731809109731814CTCTG-----31GENIChomozygous51599663
10109734004109734005GA37GENICpossibly homozygous51599664