chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183174030431740305TC2GENIChomozygous110323300
183174030531740306GC2GENIChomozygous110323302
183177789931777900GC24GENIChomozygous110323304
183177809731778098CT5GENIChomozygous110323306
183177819531778196AC10GENIChomozygous110323308
183177842731778428AT14GENIChomozygous110323312
183177868831778689GT18GENIChomozygous110323314
183177900231779003GT7GENIChomozygous110323318
183178023231780233GA17GENIChomozygous110323320
183184700731847008AT9GENIChomozygous110323322
183187754531877546AC26GENIChomozygous110832841
183189607631896077GC29GENIChomozygous110323330
183190479331904794GA16GENIChomozygous110832843
183190504031905041GA16GENIChomozygous110457903
183190506831905069AC8GENIChomozygous110457904
183190507031905071CG7GENIChomozygous110457905
183198180731981808TA13GENIChomozygous110323336
183198180931981810TC13GENIChomozygous110323338
183198488331984884GA14GENIChomozygous110832845
183201309632013097AT15GENIChomozygous110458031
183198177831981779GA18GENIChomozygous110532956
183213346532133466CT12GENIChomozygous110323342
183217501432175015GA21GENIChomozygous110458117
183217574132175742GT20GENIChomozygous110832847
183229524532295246GC24GENIChomozygous110589482
183229801232298013GT14GENIChomozygous110458235
183259402932594030CT44GENIChomozygous110532968
183262616332626164AG23GENIChomozygous110324575
183267381032673811CG28GENIChomozygous110324594
183267444932674450AC32GENIChomozygous110324596
183267577332675774AT15GENIChomozygous110324598
183269044232690443AC14GENIChomozygous110324600
183269073232690733AG19GENICpossibly homozygous110324604
183269078232690783GT19GENIChomozygous110324606
183269078332690784TG19GENIChomozygous110589484
183269084132690842AC17GENIChomozygous110589486
183269089832690899GA15GENIChomozygous110458512
183269090032690901AC15GENIChomozygous110458513
183269100632691007AC10GENIChomozygous110324608