chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
192617578926175790CT79GENICpossibly homozygous109673665
192617582226175823GA79GENICpossibly homozygous109673667
192617675926176760TA42GENICpossibly homozygous109673669
192617987126179872CG62GENIChomozygous109673673