chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123930952339309524TA19GENICpossibly homozygous50198130
123930969939309700AG17GENIChomozygous50198134
123931013239310133GA26GENICpossibly homozygous50592077
123931040139310402GA21GENICpossibly homozygous50511547
123931049939310500CA14GENICpossibly homozygous50511551
123931054139310542A-14GENICpossibly homozygous50198136
123931057839310579CCA5GENIChomozygous50451861
123931180339311804AG3GENICheterozygous50198153
123931619639316197TC12GENICpossibly homozygous50451863
123931679939316800CCGT5GENICheterozygous50542838
123931710239317103TC15GENIChomozygous50451867
123931740939317410AG7GENIChomozygous50451868
123931783739317838GA12GENICheterozygous50451869
123931785439317855TC10GENICheterozygous50198218
123931826839318275TGGTCAC-------3GENIChomozygous50451870
123931857139318572TC19GENICpossibly homozygous50451871
123931867539318676TC14GENICpossibly homozygous50451872
123931956339319564GA16GENICpossibly homozygous50451875
123931983539319836AG2GENIChomozygous50451877
123932000039320008ATGTGCAC--------3GENIChomozygous50451878
123932008239320083AC16GENICpossibly homozygous50451879
123932039439320395GA25GENICpossibly homozygous50451880
123932117939321180GA16GENIChomozygous50451881
123932121339321214CT14GENICpossibly homozygous50451882
123932194939321950CT7GENICheterozygous50198224
123932264039322641CT14GENIChomozygous50592078
123932265939322660CT9GENIChomozygous50592079
123932267439322675GA10GENICpossibly homozygous50451884
123932270639322707CT6GENICheterozygous50198227
123932321339323214TC20GENICpossibly homozygous50198229
123932342439323425TTG3INTERGENIChomozygous50198231
123932530839325313GGGGG-----1GENIChomozygous50592080