chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121933051319330514A-25GENIChomozygous50368645
121933089519330929CGCACGCACGCACGCACGCACGCACGCACGCACG----------------------------------9GENICpossibly homozygous50536689
121933115519331156GT9GENIChomozygous50368651
121933135619331357AG19GENIChomozygous50368653
121933163419331635TC16GENIChomozygous50368655
121933177119331772TC33GENIChomozygous50368657
121933210619332107TC22GENIChomozygous50368659
121933294919332950CT22GENIChomozygous50368661
121933315319333154AG23GENIChomozygous50368663
121933323519333236TC10GENIChomozygous50368665
121933332819333329TC14GENIChomozygous50098673
121933402619334027AG12GENIChomozygous50098675
121933464219334643GGGTGT4GENICheterozygous50098679
121933464219334643GGGGGTGT4GENICheterozygous50098681
121933464219334643GGGTGTGT4GENICheterozygous50597302
121933579519335796AG16GENIChomozygous50368670
121933627119336272TC12GENIChomozygous50098683
121933656519336566TTGCA5GENIChomozygous50368672
121933756019337564GCCT----5GENIChomozygous50098685
121933791719337918GA15GENIChomozygous50368674
121933893019338931TC9GENIChomozygous50098689
121934029119340292AG14GENIChomozygous50098699
121934129819341299AT31GENIChomozygous50098701
121934130019341301TG31GENIChomozygous50098703
121934147719341478AG17GENIChomozygous50098707
121934215419342159GTGGG-----13GENIChomozygous50098713
121934328819343289CT25GENIChomozygous50098719
121934413319344134GA22GENIChomozygous50368686
121934441419344415GC18GENIChomozygous50098721
121934449719344498TC22GENIChomozygous50098723
121934494419344946AC--26GENIChomozygous50098727