chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1534617473461748A-10GENIChomozygous48223867
1534686153468616AAG17GENICheterozygous48223868
1534733553473359GTGT----3GENIChomozygous48223870
1534866983486699AG36GENIChomozygous48223871
1534898893489890AG45GENICheterozygous48223872
1534900713490072AT72GENICpossibly homozygous48223873
1534978193497820A-2GENIChomozygous48223874
1535019043501905TTATA4GENIChomozygous48223875
1535091243509125A-18GENIChomozygous48223876
1535091303509131AAG13GENIChomozygous48223877
1535091723509173A-5GENIChomozygous48223878
1535098963509897GA50GENICheterozygous48223879
1535132473513248TG35GENICpossibly homozygous48692250
1535161223516123GC35GENIChomozygous48223880
1535161343516136CA--18GENICheterozygous48451904
1535163243516325C-39GENIChomozygous48223881
1535221813522182AC24GENICpossibly homozygous48223882
1535233443523345CCA19INTERGENICheterozygous48451912
1535247533524754TG52INTERGENIChomozygous48451914
1535247553524756GT54INTERGENICpossibly homozygous48451916
1535339723533973CG39INTERGENICpossibly homozygous48223883
1535440823544083C-37INTERGENIChomozygous48223885
1535441383544139AC47INTERGENICheterozygous48664580
1535441533544154GC56INTERGENICheterozygous48561592
1535441783544179CA60INTERGENICpossibly homozygous48223886