chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1221174086221174087CT26GENIChomozygous61093760
1221177638221177639AG40GENIChomozygous61093763
1221178674221178686TCTCTGTCTCTT------------18GENICpossibly homozygous61093764
1221178712221178714TG--32GENIChomozygous61093765
1221179085221179086AG28GENIChomozygous61093766
1221179272221179273TG24GENIChomozygous61093767
1221179358221179359AC27GENIChomozygous61093768
1221179362221179363AG28GENICpossibly homozygous61093769