chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4205128834205128835GA17GENIChomozygous57058213
4205129264205129265AG22GENIChomozygous57058214
4205129586205129587TTG19GENIChomozygous57058215
4205129782205129783TC15GENIChomozygous57058216
4205129956205129957CT19GENIChomozygous57058217
4205130242205130243CT20GENIChomozygous57362815
4205130304205130305CT24GENIChomozygous57058218
4205130305205130306TC24GENIChomozygous57058219
4205130578205130579CT17GENIChomozygous57058220
4205130927205130928CG16GENIChomozygous57058221
4205131056205131057TC24GENIChomozygous57058222
4205131067205131068AG27GENIChomozygous57058223
4205131439205131440GC28GENIChomozygous57058224
4205132645205132646GA13GENIChomozygous57058225
4205133026205133027GA18GENIChomozygous57362817
4205133039205133040AG18GENIChomozygous57058226
4205133447205133448GA21GENIChomozygous57058227
4205133966205133967CT12GENIChomozygous57362819
4205134011205134012TC12GENIChomozygous57058228
4205134854205134855CT24GENIChomozygous57362821
4205135577205135578CT21GENIChomozygous57362823
4205137912205137913CT1GENIChomozygous58410458
4205138221205138222TC16GENIChomozygous57058230
4205138227205138228GGTTT19GENICheterozygous57058231
4205138227205138228GGTT19GENICpossibly homozygous57362825
4205149823205149824TC28GENIChomozygous57058232
4205149920205149921TA35GENIChomozygous57058233