chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124124690124124700ATGGTATGGT----------9GENIChomozygous55728263
6124124778124124779GGT20GENIChomozygous54687102
6124128216124128217TC39GENIChomozygous54687106
6124130855124130856TC26GENIChomozygous54687109
6124132452124132453TTG40GENIChomozygous54687110
6124132455124132456GA38GENIChomozygous54687111
6124132457124132458TC36GENIChomozygous54687112
6124132458124132459TA37GENIChomozygous54687113
6124132460124132461GGC34GENIChomozygous54687114
6124133010124133011CCT23GENICpossibly homozygous55054342
6124133736124133737TC28GENIChomozygous54687117
6124133981124133982TC32GENIChomozygous54687118
6124134298124134299GA32GENICpossibly homozygous55269090
6124126380124126381CT39GENIChomozygous55269081
6124132107124132108GA38GENIChomozygous55269084
6124133857124133858AC25GENIChomozygous55269087
6124134368124134378GTGTGTGTGT----------5GENICheterozygous55728266