chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1140845519140845520GA52GENIChomozygous108259022
1140846341140846342CT58GENIChomozygous108936361
1140847133140847134AC81GENIChomozygous108936362
1140847185140847186GA78GENIChomozygous108936363
1140847446140847447GA57GENIChomozygous108936364
1140847676140847677CT74GENIChomozygous108936365
1140846531140846532G31GENICpossibly homozygous130823431
1140847868140847869CG16GENIChomozygous121085237
1140847870140847871CG16GENIChomozygous121085238
1140847872140847873CG16GENIChomozygous121085239
1140847874140847875CG16GENIChomozygous121085240
1140847876140847877CG16GENIChomozygous121085241
1140848190140848191TC56GENIChomozygous108936366
1140848394140848395CT52GENIChomozygous108936367
1140848827140848828CT63GENIChomozygous108936368
1140849499140849500GA36GENIChomozygous108259034
1140850550140850551GT58GENIChomozygous108259035
1140850659140850660GA48GENIChomozygous108259037
1140851129140851130CT51GENIChomozygous108259039
1140851141140851142AT51GENIChomozygous108259041
1140851469140851470TC36GENIChomozygous108259043
1140851904140851905CT52GENIChomozygous108259045
1140852871140852883AAAACAAAACAA49GENIChomozygous130823432
1140854214140854215C71GENIChomozygous130823433
1140855002140855003AG82GENIChomozygous108259049
1140855711140855712CT61GENIChomozygous108259051
1140848084140848084TG46GENIChomozygous127438686
1140849120140849121CA29GENICpossibly homozygous109048848
1140857565140857566TC57GENIChomozygous108259053
1140858263140858264GC72GENIChomozygous108259055
1140858312140858313AC68GENIChomozygous108259057