chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4151178533151178534GA11GENIChomozygous113395657
4151178554151178555TA11GENIChomozygous113395659
4151178565151178566TG8GENIChomozygous113243849
4151179354151179355CT18GENIChomozygous113243851
4151179396151179397TG24GENIChomozygous113243852
4151179519151179520AG21GENIChomozygous113243853
4151179608151179609GA11GENIChomozygous113243854
4151179628151179629GT5GENIChomozygous113243855
4151179634151179635AG8GENIChomozygous113395661
4151179996151179997AT11GENIChomozygous113243856
4151180357151180358AG14GENIChomozygous113243857
4151180427151180428CA4GENIChomozygous113243858
4151180444151180445CA8GENIChomozygous113395665
4151180609151180610CT24GENIChomozygous112885541
4151180806151180807GA15GENIChomozygous119575876
4151181089151181090TC22GENIChomozygous113243859
4151181368151181369AG19GENIChomozygous113243860
4151181584151181585TA8GENIChomozygous113395669
4151181711151181712AG21GENIChomozygous113243862
4151181903151181904AG17GENIChomozygous119575877
4151182137151182138GA12GENIChomozygous119575878
4151183025151183026GT30GENIChomozygous113243864
4151182832151182833AC7GENICheterozygous126120366