chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4205128834205128835GA30GENIChomozygous648375466
4205129264205129265AG34GENIChomozygous648375467
4205129586205129587TTG21GENIChomozygous756105899
4205129782205129783TC29GENIChomozygous648375468
4205129956205129957CT21GENIChomozygous648375469
4205130242205130243CT27GENIChomozygous648375470
4205130304205130305CT22GENIChomozygous648375471
4205130305205130306TC21GENIChomozygous648375472
4205130578205130579CT29GENIChomozygous648375473
4205130927205130928CG27GENIChomozygous648375474
4205131056205131057TC27GENIChomozygous648375475
4205131067205131068AG26GENIChomozygous648375476
4205131439205131440GC25GENIChomozygous648375477
4205132645205132646GA25GENIChomozygous648375478
4205133026205133027GA27GENIChomozygous648375479
4205133039205133040AG23GENIChomozygous648375480
4205133447205133448GA27GENIChomozygous648375481
4205133966205133967CT28GENIChomozygous648375482
4205134011205134012TC27GENIChomozygous648375483
4205134854205134855CT28GENIChomozygous648375484
4205135577205135578CT12GENIChomozygous648375485
4205137895205137896AATAAG2GENICheterozygous756105900
4205137897205137898AAAG2GENICheterozygous756105901
4205137912205137913CT2GENIChomozygous648375486
4205138221205138222TC12GENIChomozygous648375487
4205138227205138228GGTT12GENIChomozygous756105902
4205149823205149824TC26GENIChomozygous648375488
4205149920205149921TA20GENIChomozygous648375489