chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124124690124124700ATGGTATGGT----------4GENICheterozygous55728263
6124124778124124779GGT19GENIChomozygous54687102
6124128216124128217TC21GENIChomozygous54687106
6124130855124130856TC29GENIChomozygous54687109
6124132452124132453TTG11GENIChomozygous54687110
6124132455124132456GA11GENIChomozygous54687111
6124132457124132458TC9GENIChomozygous54687112
6124132458124132459TA9GENIChomozygous54687113
6124132460124132461GGC9GENIChomozygous54687114
6124133010124133011CCT4GENIChomozygous55054342
6124133736124133737TC14GENIChomozygous54687117
6124133981124133982TC13GENIChomozygous54687118
6124134298124134299GA25GENIChomozygous55269090
6124126380124126381CT15GENIChomozygous55269081
6124132107124132108GA30GENIChomozygous55269084
6124133857124133858AC15GENIChomozygous55269087
6124134368124134378GTGTGTGTGT----------5GENICheterozygous55728266