chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55949087859490879TA45GENIChomozygous978989536
55949624259496243AG31GENIChomozygous978989537
55949649259496493CA55GENIChomozygous978989538
55949650759496508GA60GENIChomozygous978989539
55949825659498257GA37GENIChomozygous978989540
55949964359499644TA21GENIChomozygous978989541
55950017959500180AG18GENIChomozygous978989542
55950160759501608CT25GENIChomozygous978989543
55950220759502208CA40GENIChomozygous978989544
55950224359502244CT48GENICpossibly homozygous978989545
55950230059502301GA47GENIChomozygous978989546
55950268359502684TC58GENIChomozygous978989547
55950269859502699AT61GENIChomozygous978989548
55950323259503233CT53GENIChomozygous978989549
55950324559503246CT62GENIChomozygous978989550
55950342259503423GA64GENIChomozygous978989551
55950351459503515TC45GENIChomozygous978989552
55950411659504117TC22GENICpossibly homozygous978989553
55950448859504489AG27GENIChomozygous978989554
55950483159504832CA44GENIChomozygous978989555
55950488859504889TC44GENIChomozygous978989556
55950501959505020GT41GENIChomozygous978989557
55950506259505063TA35GENIChomozygous978989558
55950519359505194TC31GENIChomozygous978989559
55950546359505464TC23GENIChomozygous978989560
55950570259505703CT42GENIChomozygous978989561
55950571859505719GA33GENIChomozygous978989562
55950584859505849CT33GENIChomozygous978989563
55950592559505926TC30GENIChomozygous978989564
55950600259506003CT51GENIChomozygous978989565
55950625659506257CT50GENIChomozygous978989566
55950699159506992GC71GENIChomozygous978989567