chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6124124778124124779GGT14GENIChomozygous54687102
6124126380124126381CT19GENIChomozygous55269081
6124128216124128217TC17GENIChomozygous54687106
6124130855124130856TC22GENIChomozygous54687109
6124132107124132108GA14GENIChomozygous55269084
6124132452124132453TTG9GENIChomozygous54687110
6124132455124132456GA9GENIChomozygous54687111
6124132457124132458TC9GENIChomozygous54687112
6124132458124132459TA9GENIChomozygous54687113
6124132460124132461GGC9GENIChomozygous54687114
6124133736124133737TC14GENIChomozygous54687117
6124133857124133858AC14GENIChomozygous55269087
6124133981124133982TC12GENIChomozygous54687118
6124129433124129434GT20GENICheterozygous56614959
6124129441124129442GC21GENICheterozygous56614961
6124129447124129448TG21GENICheterozygous56614963