chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124124778124124779GGT22GENIChomozygous54687102
6124126380124126381CT16GENIChomozygous55269081
6124128216124128217TC30GENIChomozygous54687106
6124130855124130856TC33GENIChomozygous54687109
6124132107124132108GA31GENIChomozygous55269084
6124132452124132453TTG11GENIChomozygous54687110
6124132460124132461GGC8GENIChomozygous54687114
6124133010124133011CCT4GENIChomozygous55054342
6124133736124133737TC15GENIChomozygous54687117
6124133857124133858AC18GENIChomozygous55269087
6124133981124133982TC18GENIChomozygous54687118
6124134298124134299GA27GENIChomozygous55269090
6124134364124134368GTGC----23GENICheterozygous54687120