chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135664103135664104GT15GENIChomozygous118845740
5135664105135664106GT13GENIChomozygous118858469
5135664804135664805CT16GENICpossibly homozygous114442540
5135666369135666370CT18GENIChomozygous114442544
5135668452135668453TC24GENIChomozygous114442546
5135668822135668823GA14GENIChomozygous114144691
5135669118135669119TC39GENIChomozygous114144692
5135669568135669569AG24GENIChomozygous114018310
5135669593135669594GA28GENIChomozygous114144693
5135669628135669629TC26GENIChomozygous114144694
5135669823135669824TC22GENIChomozygous114144695
5135669857135669858AC23GENIChomozygous114144696
5135672173135672174TC31GENIChomozygous114144699
5135672864135672865TC24GENIChomozygous114018312
5135673053135673054GA29GENIChomozygous114144702
5135673187135673188AG40GENIChomozygous114144703
5135673910135673911AG32GENIChomozygous114144704
5135673963135673964CT35GENIChomozygous114442548
5135674186135674187GA21GENIChomozygous114442550
5135674254135674255AG21GENIChomozygous114144705
5135674298135674299CT27GENIChomozygous114144706
5135674436135674437TC25GENIChomozygous114144707
5135674786135674787TC26GENICpossibly homozygous114144708
5135674974135674975TC22GENIChomozygous114144709
5135675084135675085CT18GENICpossibly homozygous114144710