chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1432052183205219GA12GENIChomozygous959090200
1432052253205226GT13GENIChomozygous959090201
1432056643205665CT24GENIChomozygous959090202
1432063373206338CA25GENIChomozygous959090203
1432081793208180CT16GENIChomozygous959090204
1432134853213486TG16GENIChomozygous959090205
1432150703215071AG28GENIChomozygous959090206
1432153673215368TC14GENIChomozygous959090207
1432161473216148TA32GENIChomozygous959090208
1432169313216932GT43GENIChomozygous959090209
1432184303218431AG39GENIChomozygous959090210
1432208893220890GA24GENIChomozygous959090211
1432209233220924TC30GENIChomozygous959090212
1432213363221337CT22GENIChomozygous959090213
1432226683222669CT30GENIChomozygous959090214
1432228023222803GT32GENIChomozygous959090215
1432239873223988CT39GENIChomozygous959090216
1432254713225472CT37GENIChomozygous959090217
1432293013229302TC34GENIChomozygous959090218
1432314983231499TC30GENIChomozygous959090219
1432321093232110AC24GENIChomozygous959090220
1432428213242822AC25GENIChomozygous959090221
1432451503245151CT29GENIChomozygous959090222
1432455153245516GA31GENICpossibly homozygous959090223
1432455893245590AG52GENIChomozygous959090224
1432456843245685GA62GENICpossibly homozygous959090225
1432465683246569TC20GENIChomozygous959090226
1432469093246910AG36GENIChomozygous959090227
1432470153247016TC24GENIChomozygous959090228