chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135664103135664104GT28GENIChomozygous979098732
5135664105135664106GT26GENICpossibly homozygous979098733
5135665105135665106GT17GENIChomozygous979098734
5135666369135666370CT21GENIChomozygous979098735
5135668452135668453TC65GENIChomozygous979098736
5135669118135669119TC38GENIChomozygous979098737
5135669568135669569AG28GENIChomozygous979098738
5135669593135669594GA35GENIChomozygous979098739
5135669628135669629TC37GENIChomozygous979098740
5135669823135669824TC28GENIChomozygous979098741
5135669857135669858AC21GENIChomozygous979098742
5135672173135672174TC50GENIChomozygous979098743
5135672864135672865TC56GENIChomozygous979098744
5135673053135673054GA72GENIChomozygous979098745
5135673187135673188AG65GENIChomozygous979098746
5135673910135673911AG59GENIChomozygous979098747
5135673963135673964CT70GENIChomozygous979098748
5135674186135674187GA55GENIChomozygous979098749
5135674254135674255AG53GENIChomozygous979098750
5135674298135674299CT45GENIChomozygous979098751
5135674436135674437TC44GENIChomozygous979098752
5135674786135674787TC72GENIChomozygous979098753
5135674974135674975TC39GENIChomozygous979098754
5135675084135675085CT22GENIChomozygous979098755