chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1432052183205219GA7GENIChomozygous890552090
1432052253205226GT4GENIChomozygous890552091
1432056643205665CT17GENIChomozygous890552092
1432063373206338CA11GENIChomozygous890552093
1432081793208180CT24GENIChomozygous890552094
1432083413208342TC6GENICheterozygous890552095
1432093383209339CT5GENIChomozygous890552096
1432101513210152CT4GENICheterozygous890552097
1432134853213486TG22GENICpossibly homozygous890552098
1432150703215071AG22GENIChomozygous890552099
1432153673215368TC12GENIChomozygous890552100
1432160573216058GA11GENIChomozygous890552101
1432161473216148TA9GENIChomozygous890552102
1432169313216932GT19GENIChomozygous890552103
1432184303218431AG14GENIChomozygous890552104
1432208893220890GA19GENIChomozygous890552105
1432209233220924TC21GENIChomozygous890552106
1432213363221337CT17GENIChomozygous890552107
1432226683222669CT12GENIChomozygous890552108
1432228023222803GT15GENIChomozygous890552109
1432239873223988CT20GENIChomozygous890552110
1432254713225472CT13GENIChomozygous890552111
1432266263226627GA8GENIChomozygous890552112
1432278393227840GA9GENIChomozygous890552113
1432293013229302TC7GENIChomozygous890552114
1432310853231086CT7GENIChomozygous890552115
1432314983231499TC13GENIChomozygous890552116
1432321093232110AC12GENIChomozygous890552117
1432363343236335CG13GENICheterozygous890552118
1432385783238579GC12GENICheterozygous890552119
1432428213242822AC15GENIChomozygous890552120
1432451503245151CT17GENIChomozygous890552121
1432455153245516GA21GENIChomozygous890552122
1432465683246569TC16GENIChomozygous890552123
1432469093246910AG18GENIChomozygous890552124
1432470153247016TC19GENIChomozygous890552125