chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
184058635040586351CT32GENIChomozygous110463644
184058708940587090TG46GENICpossibly homozygous110329492
184058716340587164CT23GENIChomozygous110329494
184058861240588613CA14GENIChomozygous110329496
184059143840591439CT12GENIChomozygous110463645
184059152440591525AT22GENIChomozygous110463646
184059322940593230CT7GENIChomozygous119490608
184059325540593256GA4GENIChomozygous119490609
184059325940593260AG4GENIChomozygous119490610
184059343240593433AT30GENICpossibly homozygous110728629
184059343540593436AT32GENIChomozygous110728631
184058960540589606CT24GENIChomozygous110728625
184059342940593430AT31GENICpossibly homozygous110728627
184059420140594202CT19GENIChomozygous110329502
184059545040595451GA25GENIChomozygous110329506
184059572540595726AG15GENIChomozygous110463648
184059573440595735CT16GENIChomozygous110463649
184059583840595839TC17GENIChomozygous110463650
184059600440596005AG30GENIChomozygous110329508
184059712340597124GT25GENIChomozygous110463652
184059746140597462TG25GENIChomozygous110329510