chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14104609611104609612GA44GENIChomozygous139614763
14104609835104609836AG50GENIChomozygous139614764
14104613029104613030CT56GENICpossibly homozygous139614765
14104613624104613625AC43GENIChomozygous139614766
14104614642104614643TC48GENIChomozygous139614767
14104614732104614733CT46GENIChomozygous139614768
14104614749104614750GA43GENIChomozygous139614769
14104614843104614844TA48GENIChomozygous139614770
14104615287104615288GC26GENIChomozygous139614771
14104615317104615318CT24GENIChomozygous139614772
14104615697104615698GA58GENIChomozygous139614774
14104615851104615852GA44GENIChomozygous139614775
14104616059104616060CA50GENIChomozygous139614776
14104616089104616090AT47GENIChomozygous139614777
14104617345104617346AG66GENIChomozygous139614778
14104617594104617595AG56GENIChomozygous139614779
14104618073104618074GA68GENICpossibly homozygous139614780
14104618759104618760TA41GENIChomozygous139614781