chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117306574117306575GC46GENIChomozygous116671354
8117309816117309817GC36GENIChomozygous116671360
8117309847117309848TC39GENIChomozygous116671362
8117310185117310186CA28GENIChomozygous116671364
8117310257117310258GT24GENICpossibly homozygous116671366
8117314327117314328CT25GENIChomozygous116671372
8117316415117316416TC19GENIChomozygous116671374
8117329282117329283AG16GENIChomozygous116671376
8117330763117330764CT9GENIChomozygous117912573
8117333357117333358TC41GENIChomozygous116671386
8117334379117334380GA25GENIChomozygous116671388
8117336220117336221AG32GENIChomozygous116671390
8117336341117336342AT19GENIChomozygous116671392
8117337713117337714AG37GENIChomozygous116671394
8117337751117337752CT48GENIChomozygous116671396
8117337828117337829TG40GENIChomozygous116671398
8117338602117338603GT32GENIChomozygous116671400
8117339518117339519AG51GENIChomozygous116671402
8117340326117340327AG44GENIChomozygous116671404
8117340834117340835CT38GENIChomozygous116671406
8117340854117340855CT32GENIChomozygous116671408
8117343917117343918AC47GENIChomozygous116671410
8117344187117344188GT32GENIChomozygous117912574
8117345214117345215AG18GENIChomozygous116671414