chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121334645313346454CT17GENIChomozygous115362625
121334740113347402AC16GENIChomozygous115260521
121335058313350584CT17GENIChomozygous115416916
121335241213352413TC33GENIChomozygous115260535
121335247813352479CG13GENIChomozygous115260537
121335249613352497AG7GENIChomozygous115260539
121335385113353852AG15GENIChomozygous115260541
121335508013355081TC4GENIChomozygous115416918
121335508613355087CT6GENIChomozygous115416920
121335593013355931CA7GENIChomozygous115416922
121335627013356271AG22GENIChomozygous115260549
121335630113356302GA24GENIChomozygous115416924
121335744013357441TC15GENIChomozygous115362637
121335815113358152TG25GENIChomozygous115362638
121335875713358758AG7GENIChomozygous115362639
121335892613358927CT11GENIChomozygous115260553
121335910513359106CT20GENIChomozygous115362640
121335931113359312GA21GENIChomozygous115362641
121335967213359673CA8GENIChomozygous115362642
121335975813359759AG18GENIChomozygous115362643
121335979413359795TC23GENIChomozygous115362644
121335986813359869GT17GENIChomozygous115362645
121335994713359948GA4GENIChomozygous115362646
121336176213361763AC27GENIChomozygous115362649
121335996913359970GA5GENIChomozygous115416926
121336050513360506TC22GENIChomozygous115260557
121336169513361696TC14GENIChomozygous115362648
121336243013362431CT11GENIChomozygous115416928
121336538513365386GT27GENIChomozygous115260565
121336721413367215GA22GENIChomozygous115260571