chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3114721511114721512CA28GENICpossibly homozygous882717804
3114721712114721713GT10GENIChomozygous882717805
3114721796114721797CT14GENIChomozygous882717806
3114721832114721833CG11GENIChomozygous882717807
3114722255114722256CT5GENIChomozygous882717808
3114722517114722518TC25GENIChomozygous882717809
3114722584114722585CT20GENIChomozygous882717810
3114722627114722628CT15GENIChomozygous882717811
3114722944114722945AG9GENIChomozygous882717812
3114723642114723643TC6GENIChomozygous882717813
3114723649114723650TC5GENIChomozygous882717814
3114723814114723815CT4GENIChomozygous882717815
3114723857114723858AG11GENIChomozygous882717816
3114724148114724149TC15GENIChomozygous882717817
3114724249114724250AC13GENIChomozygous882717818
3114724379114724380CG25GENIChomozygous882717819
3114724710114724711CT24GENIChomozygous882717820
3114724794114724795TC29GENIChomozygous882717821
3114724874114724875CT20GENIChomozygous882717822
3114725243114725244CG19GENIChomozygous882717823
3114725495114725496CA17GENIChomozygous882717824
3114725588114725589GA21GENIChomozygous882717825
3114726577114726578GA10GENIChomozygous882717826