chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4205128834205128835GA10GENIChomozygous528848127
4205129264205129265AG22GENIChomozygous528848128
4205129586205129587TTG14GENIChomozygous693888329
4205129782205129783TC12GENIChomozygous528848129
4205129956205129957CT18GENIChomozygous528848130
4205130242205130243CT11GENIChomozygous528848131
4205130578205130579CT16GENICpossibly homozygous528848132
4205130927205130928CG13GENIChomozygous528848133
4205131056205131057TC19GENIChomozygous528848134
4205131067205131068AG18GENIChomozygous528848135
4205131439205131440GC18GENIChomozygous528848136
4205132645205132646GA17GENIChomozygous528848137
4205133026205133027GA26GENIChomozygous532080373
4205133039205133040AG30GENIChomozygous528848138
4205133447205133448GA20GENIChomozygous528848139
4205133966205133967CT29GENIChomozygous528848140
4205134011205134012TC22GENIChomozygous528848141
4205134854205134855CT31GENIChomozygous528848142
4205135577205135578CT18GENIChomozygous528848143
4205137895205137896AATAAG4GENIChomozygous693888330
4205138221205138222TC10GENIChomozygous528848144
4205138227205138228GGTTT7GENICheterozygous693888331
4205138227205138228GGTT7GENICpossibly homozygous693888332
4205149823205149824TC34GENIChomozygous528848145
4205149920205149921TA32GENIChomozygous528848146