chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
557102065710207GA17GENICpossibly homozygous113631963
557103375710338GA19GENIChomozygous113631964
557104325710433GA13GENIChomozygous114166943
557106945710695AG24GENIChomozygous113631965
557111015711102TG13GENIChomozygous113631966
557114625711463GT17GENIChomozygous113631968
557116105711611AC21GENIChomozygous113631969
557116915711692CT13GENIChomozygous113631970
557125475712548GA20GENIChomozygous113631971
557126035712604CT23GENIChomozygous113631972
557126725712673GA11GENIChomozygous113631973
557134905713491GA12GENIChomozygous113631974
557136605713661AG23GENIChomozygous113631975
557138865713887AT15GENIChomozygous113631976
557139835713984GC17GENIChomozygous118840787
557143565714357AT9GENIChomozygous113631977
557151415715142GA11GENIChomozygous113631978
557157565715757GA16GENIChomozygous113631979
557160725716073CT10GENIChomozygous113631981
557165115716512CA20GENIChomozygous113631982
557167525716753AG20GENIChomozygous113631983
557191345719135TG5GENIChomozygous114106438
557294985729499GA7GENIChomozygous113631987
557300675730068TC14GENIChomozygous113631989
557302475730248AG16GENIChomozygous113631990