chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123930839539308400AAAAA-----4GENIChomozygous50571253
123930952339309524TA20GENIChomozygous50198130
123930969939309700AG27GENIChomozygous50198134
123931013239310133GA17GENIChomozygous50592077
123931040139310402GA18GENIChomozygous50511547
123931049939310500CA35GENIChomozygous50511551
123931054139310542A-26GENIChomozygous50198136
123931057839310579CCA20GENIChomozygous50451861
123931180339311804AG22GENIChomozygous50198153
123931254039312541T-6GENIChomozygous50610426
123931578939315790T-15GENICpossibly homozygous50198215
123931582539315826GA20GENIChomozygous50610427
123931619639316197TC22GENIChomozygous50451863
123931710239317103TC25GENIChomozygous50451867
123931740939317410AG22GENIChomozygous50451868
123931783739317838GA26GENIChomozygous50451869
123931785439317855TC25GENIChomozygous50198218
123931826839318275TGGTCAC-------40GENIChomozygous50451870
123931857139318572TC44GENIChomozygous50451871
123931867539318676TC16GENIChomozygous50451872
123931956339319564GA21GENIChomozygous50451875
123931972739319728GGTTTT16GENICheterozygous50610428
123931972739319728GGTTT16GENICheterozygous50622154
123931972739319728GGTTTTTTT16GENICheterozygous50571255
123931983539319836AG20GENIChomozygous50451877
123932000039320008ATGTGCAC--------23GENIChomozygous50451878
123932008239320083AC29GENIChomozygous50451879
123932039439320395GA29GENIChomozygous50451880
123932117939321180GA30GENIChomozygous50451881
123932121339321214CT29GENIChomozygous50451882
123932194939321950CT25GENIChomozygous50198224
123932264039322641CT29GENIChomozygous50592078
123932265939322660CT25GENIChomozygous50592079
123932267439322675GA17GENIChomozygous50451884
123932270639322707CT15GENICheterozygous50198227
123932321339323214TC25GENIChomozygous50198229
123932342439323425TTG24INTERGENICpossibly homozygous50198231
123932530839325313GGGGG-----6GENIChomozygous50592080