chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2250762815250762816AG30GENIChomozygous74535878
2250763598250763599TC27GENIChomozygous75321283
2250766307250766308AT68GENIChomozygous74535884
2250766430250766431GA54GENIChomozygous75321284
2250766441250766442GA58GENIChomozygous74535887
2250768610250768611CT57GENIChomozygous74535893
2250768931250768932CT67GENIChomozygous75321285
2250769401250769402GA45GENIChomozygous75321286
2250770530250770531GC28GENIChomozygous75321287
2250772071250772072TG53GENIChomozygous75321288
2250773227250773228CT44GENIChomozygous75321289
2250773408250773409TC59GENIChomozygous75321290
2250776655250776656CG72GENIChomozygous75321291
2250778011250778012GA37GENICpossibly homozygous75321292
2250778149250778150CT56GENIChomozygous75321293
2250778374250778375GA42GENIChomozygous75321294
2250778709250778710AG45GENIChomozygous75321295
2250778892250778893GA11GENIChomozygous75321296
2250779015250779016AT34GENIChomozygous75321297
2250779856250779857GA48GENIChomozygous74535914
2250780188250780189GA45GENIChomozygous75321298
2250780207250780208TG35GENIChomozygous74535917
2250781090250781091AG34GENIChomozygous75321299
2250782121250782122GA43GENICpossibly homozygous74535920
2250782306250782307GA46GENIChomozygous75321300
2250783670250783671CT44GENICheterozygous75321301