chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
325487232548724AG17GENIChomozygous111429064
325492832549284AG15GENIChomozygous111429065
325509322550933AG14GENIChomozygous111429066
325511902551190TGCTTCCAGACAGGGGCTGTGCACAGGCTAACGTCCCCATGGCGACGC11GENIChomozygous127844480
325514132551414CT30GENIChomozygous111429067
325526152552616GA21GENIChomozygous111429068
325529532552954CA19GENIChomozygous111429069
325537102553711AG17GENIChomozygous111429070
325537232553724AG17GENIChomozygous111429071
325537372553738AG15GENIChomozygous111429072
325537442553745AG16GENIChomozygous111429073
325542372554238CT16GENICpossibly homozygous111429074
325547052554706CG23GENIChomozygous111429075
325553502555351CA18GENIChomozygous111429077
325554512555452AG8GENIChomozygous111429078
325558572555858CT23GENIChomozygous111429079
325561922556193CT20GENIChomozygous111429080
325562712556272CT22GENIChomozygous111429081
325569622556963GA17GENIChomozygous125954366
325573532557354AC20GENIChomozygous111429082
325586692558670GA17GENIChomozygous111429083
325586772558678TC15GENIChomozygous111429084
325586942558695AT15GENIChomozygous111429085
325588612558862AT17GENIChomozygous111429086
325593902559391TC14GENIChomozygous111429087
325597222559723AC19GENICheterozygous135260827
325597282559731TGA19GENICheterozygous135259914
325551212555121GCACCCGGGGGCTG12GENIChomozygous127844481
325587162558723TTTTTGG11GENIChomozygous127844482
325596932559699TGCTGA14GENICheterozygous135259913
325597342559751TGTGACGTATAGGAGGG19GENICheterozygous135259915
325608002560801G16GENIChomozygous127844484
325637432563743TC12GENIChomozygous127844485
325675482567549GA22GENIChomozygous111429092