chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121933051319330514A-9GENIChomozygous50368645
121933115519331156GT8GENIChomozygous50368651
121933135619331357AG8GENIChomozygous50368653
121933163419331635TC6GENIChomozygous50368655
121933177119331772TC11GENIChomozygous50368657
121933210619332107TC12GENIChomozygous50368659
121933294919332950CT3GENIChomozygous50368661
121933315319333154AG4GENIChomozygous50368663
121933323519333236TC7GENIChomozygous50368665
121933332819333329TC7GENIChomozygous50098673
121933402619334027AG12GENIChomozygous50098675
121933464219334643GGGGGTGT6GENICheterozygous50098681
121933464219334643GGGTGTGT6GENICheterozygous50597302
121933089519330929CGCACGCACGCACGCACGCACGCACGCACGCACG----------------------------------1GENIChomozygous50536689
121933579519335796AG8GENIChomozygous50368670
121933627119336272TC6GENIChomozygous50098683
121933756019337564GCCT----6GENIChomozygous50098685
121933791719337918GA7GENIChomozygous50368674
121933893019338931TC9GENIChomozygous50098689
121934029119340292AG11GENIChomozygous50098699
121934129819341299AT18GENIChomozygous50098701
121934130019341301TG19GENIChomozygous50098703
121934147719341478AG4GENIChomozygous50098707
121934215419342159GTGGG-----8GENIChomozygous50098713
121934328819343289CT10GENIChomozygous50098719
121934413319344134GA9GENIChomozygous50368686
121934441419344415GC12GENIChomozygous50098721
121934449719344498TC10GENIChomozygous50098723
121934494419344946AC--14GENIChomozygous50098727