chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101697069616970697TC56GENICpossibly homozygous116739337
101697207716972078TC44GENIChomozygous117177217
101697231916972320AG73GENIChomozygous116995034
101697283716972838GA41GENIChomozygous116995035
101697310616973107AG79GENIChomozygous116995036
101697311016973111TA76GENIChomozygous116995037