chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123930839539308400AAAAA-----8GENICheterozygous50571253
123930969939309700AG29GENIChomozygous50198134
123930952339309524TA29GENIChomozygous50198130
123931040139310402GA30GENIChomozygous50511547
123931049939310500CA20GENIChomozygous50511551
123931054139310542A-19GENIChomozygous50198136
123931057839310579CCA11GENIChomozygous50451861
123931180339311804AG17GENIChomozygous50198153
123931013239310133GA29GENIChomozygous50592077
123931254039312541T-4GENIChomozygous50610426
123931578939315790T-10GENIChomozygous50198215
123931582539315826GA14GENIChomozygous50610427
123931619639316197TC24GENIChomozygous50451863
123931710239317103TC21GENIChomozygous50451867
123931740939317410AG19GENIChomozygous50451868
123931783739317838GA33GENIChomozygous50451869
123931785439317855TC31GENIChomozygous50198218
123931826839318275TGGTCAC-------29GENIChomozygous50451870
123931857139318572TC27GENIChomozygous50451871
123931867539318676TC32GENIChomozygous50451872
123931956339319564GA16GENIChomozygous50451875
123931972739319728GGTTT2GENICheterozygous50622154
123931972739319728GGTTTTTTT2GENICheterozygous50571255
123931983539319836AG20GENIChomozygous50451877
123932000039320008ATGTGCAC--------25GENIChomozygous50451878
123932008239320083AC27GENIChomozygous50451879
123932039439320395GA31GENIChomozygous50451880
123932117939321180GA23GENIChomozygous50451881
123932121339321214CT19GENIChomozygous50451882
123932194939321950CT9GENIChomozygous50198224
123932264039322641CT20GENIChomozygous50592078
123932265939322660CT15GENIChomozygous50592079
123932267439322675GA10GENIChomozygous50451884
123932270639322707CT2GENICheterozygous50198227
123932321339323214TC22GENIChomozygous50198229
123932342439323425TTG15INTERGENICpossibly homozygous50198231
123932530839325313GGGGG-----6GENIChomozygous50592080