chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124124690124124700ATGGTATGGT----------2GENIChomozygous55728263
6124124778124124779GGT16GENIChomozygous54687102
6124128216124128217TC15GENIChomozygous54687106
6124130855124130856TC18GENIChomozygous54687109
6124132452124132453TTG18GENIChomozygous54687110
6124132455124132456GA18GENIChomozygous54687111
6124132457124132458TC19GENIChomozygous54687112
6124132458124132459TA19GENIChomozygous54687113
6124132460124132461GGC19GENIChomozygous54687114
6124133010124133011CCT9GENICpossibly homozygous55054342
6124133736124133737TC32GENIChomozygous54687117
6124133981124133982TC19GENIChomozygous54687118
6124134298124134299GA18GENIChomozygous55269090
6124126380124126381CT35GENIChomozygous55269081
6124132107124132108GA26GENIChomozygous55269084
6124133857124133858AC19GENIChomozygous55269087
6124134368124134378GTGTGTGTGT----------5GENICheterozygous55728266