chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
182491856224918563CA19GENICheterozygous46394049
182491856224918563CG19GENICheterozygous46831844
182492164524921646CT12GENIChomozygous46394050
182492170324921704AT10GENIChomozygous46394052
182492188124921882GA18GENIChomozygous46394053
182492196324921964CCTG26GENIChomozygous46394055
182492218724922188AC21GENIChomozygous46394057
182492232224922323A-17GENIChomozygous46394058
182492234624922347AT19GENIChomozygous46394060
182492265324922654AG26GENIChomozygous46394061
182492649224926493TC21GENIChomozygous46394064
182492672324926724TC13GENIChomozygous46394066
182492826024928261C-12GENIChomozygous46394068