chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135664103135664104GT11GENIChomozygous958065498
5135664105135664106GT12GENIChomozygous958065499
5135664804135664805CT21GENIChomozygous958065500
5135665105135665106GT20GENIChomozygous958065501
5135666369135666370CT17GENIChomozygous958065502
5135668452135668453TC17GENIChomozygous958065503
5135669118135669119TC45GENIChomozygous958065504
5135669568135669569AG26GENIChomozygous958065505
5135669593135669594GA20GENIChomozygous958065506
5135669628135669629TC18GENIChomozygous958065507
5135669823135669824TC19GENIChomozygous958065508
5135669857135669858AC19GENIChomozygous958065509
5135672173135672174TC32GENIChomozygous958065510
5135672864135672865TC34GENIChomozygous958065511
5135673053135673054GA34GENIChomozygous958065512
5135673187135673188AG39GENIChomozygous958065513
5135673910135673911AG37GENIChomozygous958065514
5135673963135673964CT26GENIChomozygous958065515
5135674186135674187GA30GENIChomozygous958065516
5135674254135674255AG24GENIChomozygous958065517
5135674298135674299CT20GENIChomozygous958065518
5135674436135674437TC18GENIChomozygous958065519
5135674786135674787TC28GENIChomozygous958065520
5135674974135674975TC27GENIChomozygous958065521
5135675084135675085CT21GENIChomozygous958065522