chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134468818134468819CT46GENIChomozygous114143968
5134469169134469170AG46GENIChomozygous114016894
5134470622134470623GA44GENIChomozygous114143969
5134471241134471242GA39GENIChomozygous114143970
5134473057134473058GC20GENIChomozygous114143982
5134473137134473138TG28GENIChomozygous114016900
5134473998134473999AG45GENIChomozygous114143983
5134474383134474384GA49GENIChomozygous114143984
5134476413134476414AG39GENIChomozygous114016903
5134476884134476885CT33GENIChomozygous114016904
5134477258134477259GA45GENICpossibly homozygous114143985
5134477293134477294GA47GENIChomozygous114143986
5134477506134477507AG40GENIChomozygous114016905
5134477737134477738AG35GENIChomozygous114143987
5134471019134471019GGATGAGTCCTGTAGACTTT35GENIChomozygous128241780