chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124124778124124779GGT13GENIChomozygous54687102
6124125125124125126AG19GENIChomozygous54687103
6124127497124127498GA20GENIChomozygous54687104
6124128152124128153CT7GENICpossibly homozygous54687105
6124128216124128217TC19GENIChomozygous54687106
6124130484124130485AG9GENIChomozygous54687107
6124130660124130661CA9GENICpossibly homozygous54687108
6124130855124130856TC26GENIChomozygous54687109
6124132452124132453TTG1GENIChomozygous54687110
6124132500124132501CT17GENIChomozygous54687115
6124133010124133011CCTTT2GENIChomozygous54687116
6124133736124133737TC24GENIChomozygous54687117
6124133981124133982TC29GENIChomozygous54687118
6124134406124134407GA7GENICpossibly homozygous54687122