chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4205128834205128835GA24GENIChomozygous606120282
4205129264205129265AG19GENIChomozygous606120283
4205129586205129587TTG29GENIChomozygous733127455
4205129782205129783TC44GENIChomozygous606120284
4205129956205129957CT33GENIChomozygous606120285
4205130304205130305CT24GENIChomozygous606120286
4205130305205130306TC24GENIChomozygous606120287
4205130578205130579CT25GENIChomozygous606120288
4205130927205130928CG30GENIChomozygous606120289
4205131056205131057TC37GENIChomozygous606120290
4205131067205131068AG37GENIChomozygous606120291
4205131439205131440GC21GENIChomozygous606120292
4205132557205132558GA30GENIChomozygous608756461
4205132645205132646GA31GENIChomozygous606120293
4205133039205133040AG24GENIChomozygous606120294
4205133447205133448GA26GENIChomozygous606120295
4205134011205134012TC27GENIChomozygous606120296
4205137925205137933ATATATAG--------1GENIChomozygous733127456
4205138221205138222TC22GENIChomozygous606120297
4205138227205138228GGTT17GENICheterozygous733127457
4205138227205138228GGTTT17GENICpossibly homozygous733127458
4205149823205149824TC20GENIChomozygous606120298
4205149920205149921TA31GENIChomozygous606120299