chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1235188152235188153CT21GENIChomozygous61610104
1235188762235188763TTACAC6GENICheterozygous61610105
1235192220235192221CG13GENIChomozygous61610107
1235192689235192690AG32GENIChomozygous61610108
1235192976235192977TC24GENIChomozygous61610109
1235195179235195180CT12GENIChomozygous61610110
1235195551235195552TA29GENIChomozygous61610111
1235195846235195847T-17GENIChomozygous61610112
1235195860235195861A-19GENIChomozygous61610113
1235196631235196632CA21GENIChomozygous61610114
1235196966235196967AT18GENIChomozygous61610115
1235197943235197947TGTG----24GENIChomozygous61610116
1235198730235198746GAAAGAACAAACGAAC----------------11GENIChomozygous62415672
1235199168235199169AAG19GENIChomozygous61610118
1235199602235199603CCA22GENIChomozygous61610119
1235199605235199606T-16GENIChomozygous61323022
1235199608235199609T-16GENIChomozygous62415674
1235199611235199612T-16GENIChomozygous62415676
1235199614235199615T-16GENIChomozygous62415678
1235199617235199618T-16GENIChomozygous62415680
1235199620235199639TCATCATCATCATCATCAT-------------------15GENIChomozygous62556817
1235199756235199757AAC24GENIChomozygous61610120
1235199757235199758AC25GENIChomozygous62104962
1235200019235200020AG29GENIChomozygous61610121
1235200130235200131GA13GENIChomozygous61610122