chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14104609611104609612GA16GENIChomozygous139614763
14104609835104609836AG21GENIChomozygous139614764
14104611865104611869AATT10GENIChomozygous140913741
14104613029104613030CT20GENIChomozygous139614765
14104613624104613625AC21GENIChomozygous139614766
14104614642104614643TC33GENIChomozygous139614767
14104614732104614733CT35GENIChomozygous139614768
14104614749104614750GA34GENIChomozygous139614769
14104614843104614844TA22GENIChomozygous139614770
14104615287104615288GC18GENIChomozygous139614771
14104615317104615318CT11GENIChomozygous139614772
14104615697104615698GA31GENIChomozygous139614774
14104615851104615852GA19GENIChomozygous139614775
14104616059104616060CA23GENIChomozygous139614776
14104616089104616090AT26GENICpossibly homozygous139614777
14104617345104617346AG14GENIChomozygous139614778
14104617594104617595AG21GENIChomozygous139614779
14104618073104618074GA30GENIChomozygous139614780
14104618759104618760TA29GENIChomozygous139614781