chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71265310912653110GT21GENIChomozygous115570305
71265336312653364CT21GENIChomozygous115570306
71265343212653433AT23GENIChomozygous115570307
71265382012653820G18GENIChomozygous128435832
71265384812653849GA18GENIChomozygous115570308
71265501612655017TG12GENIChomozygous115570309
71265549712655498C10GENIChomozygous128435833
71265622812656229TC20GENIChomozygous115570310
71265765612657657GA11GENIChomozygous115570312
71265876212658762GGGCCTTGCGCTTCCTAG7GENIChomozygous128435837
71265726512657266C14GENIChomozygous128435834
71265726712657270TTC16GENIChomozygous128435835
71265728412657284T16GENIChomozygous128435836
71265897012658971GA23GENIChomozygous115570313
71265936312659364C19GENICheterozygous128435838
71265970312659704TC19GENIChomozygous115570315
71266022412660225TC14GENIChomozygous115570316
71266024312660244AG14GENIChomozygous115570317
71266113212661133CT16GENIChomozygous115570318
71266127012661271AG15GENIChomozygous115570319
71266216912662170AT21GENIChomozygous115570320
71266244512662446TC22GENIChomozygous115570322
71266246612662467GA25GENIChomozygous115570323
71266251012662511CG23GENIChomozygous115570324
71266377512663775G24GENIChomozygous128435839