chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
146113769461137695GC13GENIChomozygous113476870
146113931961139320AG15GENIChomozygous113476872
146114491461144915AG14GENIChomozygous113476876
146114866361148664GT4GENIChomozygous125917676
146114888161148882TG4GENIChomozygous125917677
146115175661151757GT11GENIChomozygous125917678
146115522161155222AG11GENIChomozygous125917679
146115700561157006GA14GENIChomozygous125917680
146116262561162626AG22GENICpossibly homozygous125917681
146116388661163887CT11GENIChomozygous113476878
146116441361164414TC10GENIChomozygous113476880
146117204361172044AG10GENIChomozygous113476882
146117361461173615GA6GENIChomozygous113476884
146115126761151268CT10GENIChomozygous113945481