chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1432052183205219GA15GENIChomozygous950770872
1432052253205226GT16GENIChomozygous950770873
1432056643205665CT32GENIChomozygous950770874
1432063373206338CA15GENIChomozygous950770875
1432081793208180CT16GENIChomozygous950770876
1432134853213486TG22GENIChomozygous950770877
1432150703215071AG26GENIChomozygous950770878
1432153673215368TC16GENIChomozygous950770879
1432160573216058GA11GENIChomozygous950770880
1432161473216148TA8GENIChomozygous950770881
1432169313216932GT18GENIChomozygous950770882
1432184303218431AG22GENIChomozygous950770883
1432208893220890GA9GENIChomozygous950770884
1432209233220924TC10GENIChomozygous950770885
1432213363221337CT26GENIChomozygous950770886
1432226683222669CT13GENIChomozygous950770887
1432228023222803GT28GENIChomozygous950770888
1432239873223988CT7GENIChomozygous950770889
1432254713225472CT19GENIChomozygous950770890
1432266743226675AG15GENIChomozygous950770891
1432293013229302TC15GENIChomozygous950770892
1432314983231499TC15GENIChomozygous950770893
1432321093232110AC25GENIChomozygous950770894
1432428213242822AC12GENIChomozygous950770895
1432451503245151CT26GENIChomozygous950770896
1432455153245516GA29GENIChomozygous950770897
1432455893245590AG34GENIChomozygous950770898
1432456843245685GA22GENIChomozygous950770899
1432465683246569TC35GENIChomozygous950770900
1432469093246910AG15GENIChomozygous950770901
1432470153247016TC18GENIChomozygous950770902