chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135664103135664104GT10GENIChomozygous932218808
5135664105135664106GT9GENIChomozygous932218809
5135664804135664805CT12GENIChomozygous932218810
5135665105135665106GT11GENICpossibly homozygous932218811
5135668452135668453TC3GENIChomozygous932218812
5135668822135668823GA8GENIChomozygous932218813
5135669118135669119TC11GENIChomozygous932218814
5135669568135669569AG7GENIChomozygous932218815
5135669593135669594GA7GENIChomozygous932218816
5135669628135669629TC8GENIChomozygous932218817
5135669823135669824TC12GENIChomozygous932218818
5135669857135669858AC9GENIChomozygous932218819
5135672173135672174TC17GENIChomozygous932218820
5135672864135672865TC9GENIChomozygous932218821
5135673053135673054GA8GENIChomozygous932218822
5135673187135673188AG11GENIChomozygous932218823
5135673910135673911AG15GENIChomozygous932218824
5135673963135673964CT11GENIChomozygous932218825
5135674186135674187GA10GENIChomozygous932218826
5135674254135674255AG12GENIChomozygous932218827
5135674298135674299CT15GENIChomozygous932218828
5135674436135674437TC5GENIChomozygous932218829
5135674786135674787TC9GENIChomozygous932218830
5135674974135674975TC11GENIChomozygous932218831
5135675084135675085CT10GENIChomozygous932218832