chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123930839539308400AAAAA-----7GENIChomozygous50571253
123930952339309524TA25GENIChomozygous50198130
123930969939309700AG22GENIChomozygous50198134
123931013239310133GA19GENIChomozygous50592077
123931040139310402GA18GENIChomozygous50511547
123931049939310500CA32GENIChomozygous50511551
123931054139310542A-21GENIChomozygous50198136
123931057839310579CCA14GENIChomozygous50451861
123931180339311804AG17GENIChomozygous50198153
123931254039312541T-4GENIChomozygous50610426
123931578939315790T-8GENIChomozygous50198215
123931582539315826GA21GENIChomozygous50610427
123931619639316197TC28GENIChomozygous50451863
123931710239317103TC13GENIChomozygous50451867
123931740939317410AG18GENIChomozygous50451868
123931783739317838GA26GENIChomozygous50451869
123931785439317855TC23GENIChomozygous50198218
123931826839318275TGGTCAC-------15GENIChomozygous50451870
123931857139318572TC17GENIChomozygous50451871
123931867539318676TC27GENIChomozygous50451872
123931956339319564GA15GENIChomozygous50451875
123931972739319728GGTTTT5GENIChomozygous50610428
123931983539319836AG16GENIChomozygous50451877
123932000039320008ATGTGCAC--------28GENIChomozygous50451878
123932008239320083AC11GENIChomozygous50451879
123932039439320395GA21GENIChomozygous50451880
123932117939321180GA15GENIChomozygous50451881
123932121339321214CT14GENIChomozygous50451882
123932194939321950CT21GENIChomozygous50198224
123932264039322641CT15GENIChomozygous50592078
123932265939322660CT12GENIChomozygous50592079
123932267439322675GA9GENIChomozygous50451884
123932270639322707CT5GENICheterozygous50198227
123932321339323214TC24GENIChomozygous50198229
123932342439323425TTG29INTERGENICpossibly homozygous50198231
123932530839325313GGGGG-----1GENIChomozygous50592080