chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124124690124124700ATGGTATGGT----------1GENIChomozygous55728263
6124124778124124779GGT18GENIChomozygous54687102
6124128216124128217TC20GENIChomozygous54687106
6124130855124130856TC27GENIChomozygous54687109
6124132452124132453TTG36GENIChomozygous54687110
6124132455124132456GA35GENIChomozygous54687111
6124132457124132458TC36GENIChomozygous54687112
6124132458124132459TA36GENIChomozygous54687113
6124126380124126381CT35GENIChomozygous55269081
6124132107124132108GA29GENIChomozygous55269084
6124132460124132461GGC34GENIChomozygous54687114
6124133736124133737TC35GENIChomozygous54687117
6124133857124133858AC22GENIChomozygous55269087
6124133981124133982TC30GENIChomozygous54687118
6124134298124134299GA36GENIChomozygous55269090
6124134368124134378GTGTGTGTGT----------9GENICheterozygous55728266
6124133010124133011CCT12GENICheterozygous55054342