chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124124690124124700ATGGTATGGT----------1GENIChomozygous55728263
6124124778124124779GGT10GENIChomozygous54687102
6124126380124126381CT25GENIChomozygous55269081
6124128216124128217TC24GENIChomozygous54687106
6124130855124130856TC27GENIChomozygous54687109
6124132107124132108GA31GENIChomozygous55269084
6124132452124132453TTG29GENIChomozygous54687110
6124132455124132456GA29GENIChomozygous54687111
6124132457124132458TC28GENIChomozygous54687112
6124132458124132459TA28GENIChomozygous54687113
6124132460124132461GGC26GENIChomozygous54687114
6124133010124133011CCT9GENICpossibly homozygous55054342
6124133736124133737TC32GENIChomozygous54687117
6124133857124133858AC16GENIChomozygous55269087
6124133981124133982TC28GENIChomozygous54687118
6124134298124134299GA22GENICpossibly homozygous55269090
6124134368124134378GTGTGTGTGT----------6GENICheterozygous55728266
6124134370124134378GTGTGTGT--------6GENICheterozygous55910390