chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4100941787100941788CG24GENIChomozygous112798938
4100943416100943417CT15GENIChomozygous112798940
4100947234100947235GA16GENIChomozygous112798942
4100949072100949073GA27GENIChomozygous112798944
4100961324100961325TC18GENIChomozygous112798946
4100963380100963381AG4GENIChomozygous113044784
4100963428100963429CA12GENIChomozygous112798948
4100963449100963450CA18GENIChomozygous112798950
4100963551100963552TG9GENIChomozygous112798952
4100963632100963633GC19GENIChomozygous112798954
4100963686100963687TC28GENICheterozygous113146433
4100964762100964763CT21GENICheterozygous113146435
4100978054100978055CA15GENICheterozygous112798958
4100989174100989175TG28GENICheterozygous113146437
4100993770100993771CT18GENIChomozygous113146439
4101004824101004825TC114GENICheterozygous113146441
4101005056101005057CA67GENICheterozygous113146443
4101005196101005197TC37GENICheterozygous112798960
4101009933101009934AG21GENICheterozygous113044794
4101026554101026555AG28GENIChomozygous113146445
4101048817101048818CT15GENIChomozygous112798968
4101048910101048911TC11GENIChomozygous112798970
4101049171101049172AT10GENIChomozygous112798972
4101049206101049207CA11GENIChomozygous112798974
4101049240101049241TA5GENIChomozygous112798976
4101091614101091615TA10GENIChomozygous112798984
4101094333101094334GC10GENIChomozygous112798986
4101094338101094339GC10GENIChomozygous112798988
4101094982101094983TC35GENICheterozygous112798990
4101118761101118762AC3GENIChomozygous113044826
4101118768101118769CT4GENIChomozygous113044828
4101118770101118771GA4GENIChomozygous113044830
4101118802101118803AG8GENIChomozygous112798996
4101118809101118810CA8GENIChomozygous112798998
4101118815101118816AT8GENIChomozygous112799000
4101127295101127296AC9GENIChomozygous112799002
4101151463101151464CA20GENICheterozygous113146447
4101154440101154441GC48GENICheterozygous112799008
4101154463101154464GA57GENICheterozygous112799010
4101154487101154488AG62GENICheterozygous112799012