chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105562602155626022TC21GENIChomozygous116602691
105562626755626268TG22GENIChomozygous116602693
105562661655626617CT15GENIChomozygous116934877
105562756655627567CA18GENIChomozygous116782698
105562795855627959AG12GENIChomozygous116782700
105562823355628234GA19GENIChomozygous116782702
105562859755628598GA13GENICpossibly homozygous116782704
105562887355628874TG18GENIChomozygous116782706
105563002855630029TC13GENIChomozygous116934879
105563044555630446AG17GENIChomozygous116782708
105563146555631466AT11GENIChomozygous118038940
105562836655628366CTT16GENIChomozygous128818981
105563150155631501CC9GENIChomozygous131094353
105563225255632252A17GENIChomozygous128818984