chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105562602155626022TC43GENIChomozygous116602691
105562626755626268TG48GENIChomozygous116602693
105562661655626617CT30GENIChomozygous116934877
105562756655627567CA49GENIChomozygous116782698
105562795855627959AG56GENIChomozygous116782700
105562823355628234GA55GENIChomozygous116782702
105562859755628598GA64GENIChomozygous116782704
105562887355628874TG59GENICpossibly homozygous116782706
105563002855630029TC71GENIChomozygous116934879
105563044555630446AG57GENIChomozygous116782708
105563146555631466AT34GENIChomozygous118038940
105562836655628366CTT53GENIChomozygous128818981
105563225255632252A59GENIChomozygous128818984
105563150155631501CC36GENICpossibly homozygous131094353