chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121933051319330514A-17GENIChomozygous50368645
121933089519330929CGCACGCACGCACGCACGCACGCACGCACGCACG----------------------------------5GENICheterozygous50536689
121933115519331156GT16GENICpossibly homozygous50368651
121933135619331357AG20GENIChomozygous50368653
121933163419331635TC19GENIChomozygous50368655
121933177119331772TC28GENIChomozygous50368657
121933210619332107TC14GENIChomozygous50368659
121933294919332950CT29GENIChomozygous50368661
121933315319333154AG13GENIChomozygous50368663
121933323519333236TC13GENIChomozygous50368665
121933332819333329TC9GENIChomozygous50098673
121933402619334027AG16GENIChomozygous50098675
121933464219334643GGGTGT6GENICheterozygous50098679
121933464219334643GGGGGTGT6GENICheterozygous50098681
121933464219334643GGGGGT6GENICheterozygous50607196
121933579519335796AG20GENIChomozygous50368670
121933627119336272TC19GENIChomozygous50098683
121933656519336566TTGCA8GENIChomozygous50368672
121933756019337564GCCT----17GENIChomozygous50098685
121933791719337918GA18GENIChomozygous50368674
121933893019338931TC8GENIChomozygous50098689
121934029119340292AG11GENIChomozygous50098699
121934129819341299AT19GENIChomozygous50098701
121934130019341301TG19GENIChomozygous50098703
121934147719341478AG27GENIChomozygous50098707
121934215419342159GTGGG-----15GENIChomozygous50098713
121934328819343289CT27GENIChomozygous50098719
121934413319344134GA24GENIChomozygous50368686
121934441419344415GC11GENIChomozygous50098721
121934449719344498TC23GENIChomozygous50098723
121934494419344946AC--40GENIChomozygous50098727