chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18081613580816140GGGGA19GENICpossibly homozygous145234194
18081810480818108TTTA36GENIChomozygous145234195
18081844680818447CT37GENIChomozygous145273794
18081887380818873C38GENIChomozygous145234196
18082040480820405CT27GENIChomozygous145273795
18082053980820540TC37GENIChomozygous145273796
18082065880820659TC33GENIChomozygous145273797
18082136980821370TC18GENIChomozygous145273798
18082180380821804TC32GENIChomozygous145273799
18082200480822004GGCAGAAGACG39GENIChomozygous145234197
18082396880823969CA17GENICpossibly homozygous145273800