chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109727756109727757GA28GENIChomozygous51599659
10109730194109730196TT--5GENICheterozygous51599660
10109730195109730196T-5GENICheterozygous51599661
10109730311109730312TTTTTTG18GENICpossibly homozygous51599662
10109730656109730664ACACACAC--------1GENIChomozygous52814588
10109731809109731814CTCTG-----38GENIChomozygous51599663
10109734004109734005GA28GENIChomozygous51599664