chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73190426531904266GT45GENIChomozygous53863029
73190483131904832GA30GENIChomozygous53863030
73190484731904848AAG22GENIChomozygous53863031
73190484931904850AAT14GENIChomozygous53863032
73190485031904851GGGT14GENIChomozygous53863033
73190485831904859TC24GENIChomozygous53863034
73190628431906285G-25GENIChomozygous53863035
73190628731906288AC27GENICpossibly homozygous53863036
73190703131907032AC65GENICpossibly homozygous53863038
73190881331908814GA48GENIChomozygous53863039
73190888431908885TC30GENIChomozygous53863040
73191012631910127CT71GENIChomozygous53863041
73191031931910329TGTGTGTGTC----------27GENIChomozygous53863042
73191032531910326T-40GENICheterozygous53863043
73191073831910739TTGGGTTGGTGGGG19GENIChomozygous53863044