chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1224873078224873079TC17GENICpossibly homozygous61100565
1224874019224874020TC10GENICpossibly homozygous61100566
1224874035224874036TC15GENIChomozygous61100567
1224875085224875086TC22GENICpossibly homozygous61100568