chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1640427516404276CT19GENICpossibly homozygous591908659
X1640522616405227AG14GENIChomozygous591908660
X1640598216405983GC12GENIChomozygous591908661
X1640620316406204A-11GENIChomozygous726268411