chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121933051319330514A-13GENIChomozygous50368645
121933115519331156GT7GENIChomozygous50368651
121933135619331357AG16GENICpossibly homozygous50368653
121933163419331635TC26GENIChomozygous50368655
121933177119331772TC19GENICpossibly homozygous50368657
121933210619332107TC16GENIChomozygous50368659
121933294919332950CT15GENICpossibly homozygous50368661
121933315319333154AG7GENIChomozygous50368663
121933323519333236TC11GENICpossibly homozygous50368665
121933332819333329TC19GENIChomozygous50098673
121933402619334027AG3GENIChomozygous50098675
121933579519335796AG22GENICpossibly homozygous50368670
121933627119336272TC25GENICpossibly homozygous50098683
121933656519336566TTGCA1GENIChomozygous50368672
121933756019337564GCCT----3GENIChomozygous50098685
121933791719337918GA15GENIChomozygous50368674
121933893019338931TC11GENIChomozygous50098689
121934029119340292AG13GENICpossibly homozygous50098699
121934129819341299AT7GENIChomozygous50098701
121934130019341301TG9GENIChomozygous50098703
121934147719341478AG18GENIChomozygous50098707
121934215419342159GTGGG-----8GENIChomozygous50098713
121934328819343289CT19GENICpossibly homozygous50098719
121934413319344134GA17GENIChomozygous50368686
121934441419344415GC21GENIChomozygous50098721
121934449719344498TC8GENICpossibly homozygous50098723
121934494419344946AC--10GENIChomozygous50098727