chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140845519140845520GA15GENIChomozygous108259022
1140846341140846342CT25GENIChomozygous108936361
1140846531140846532G18GENIChomozygous130823431
1140847133140847134AC25GENIChomozygous108936362
1140847185140847186GA17GENIChomozygous108936363
1140847446140847447GA23GENIChomozygous108936364
1140847676140847677CT18GENIChomozygous108936365
1140848190140848191TC15GENIChomozygous108936366
1140848394140848395CT14GENIChomozygous108936367
1140848827140848828CT23GENIChomozygous108936368
1140849120140849121CA21GENICpossibly homozygous109048848
1140849499140849500GA15GENIChomozygous108259034
1140850550140850551GT18GENIChomozygous108259035
1140850659140850660GA16GENIChomozygous108259037
1140851129140851130CT18GENIChomozygous108259039
1140851141140851142AT21GENIChomozygous108259041
1140851904140851905CT9GENIChomozygous108259045
1140852871140852883AAAACAAAACAA11GENIChomozygous130823432
1140848084140848084TG10GENIChomozygous127438686
1140854214140854215C18GENIChomozygous130823433
1140855002140855003AG18GENIChomozygous108259049
1140855711140855712CT19GENIChomozygous108259051
1140857565140857566TC14GENIChomozygous108259053
1140858263140858264GC23GENIChomozygous108259055
1140858312140858313AC20GENICpossibly homozygous108259057