chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4205128834205128835GA11GENIChomozygous640896031
4205129264205129265AG21GENIChomozygous640896032
4205129586205129587TTG14GENIChomozygous751566088
4205129782205129783TC13GENIChomozygous640896033
4205129956205129957CT14GENIChomozygous640896034
4205130242205130243CT6GENIChomozygous640896035
4205130304205130305CT15GENIChomozygous640896036
4205130305205130306TC15GENIChomozygous640896037
4205130578205130579CT15GENIChomozygous640896038
4205130927205130928CG13GENIChomozygous640896039
4205131056205131057TC19GENIChomozygous640896040
4205131067205131068AG17GENIChomozygous640896041
4205131439205131440GC20GENIChomozygous640896042
4205132645205132646GA17GENIChomozygous640896043
4205133026205133027GA22GENIChomozygous640896044
4205133039205133040AG22GENIChomozygous640896045
4205133447205133448GA19GENIChomozygous640896046
4205133966205133967CT29GENIChomozygous640896047
4205134011205134012TC22GENIChomozygous640896048
4205134854205134855CT27GENIChomozygous640896049
4205135577205135578CT14GENIChomozygous640896050
4205137895205137896AATAAG3GENIChomozygous751566089
4205137912205137913CT3GENIChomozygous640896051
4205137948205137949GGGA3GENICheterozygous751566090
4205138221205138222TC9GENIChomozygous640896052
4205138227205138228GGTT8GENICpossibly homozygous751566091
4205138227205138228GGTTT8GENICheterozygous751566092
4205149823205149824TC24GENIChomozygous640896053
4205149920205149921TA22GENIChomozygous640896054