chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135664103135664104GT22GENIChomozygous955091222
5135664105135664106GT23GENIChomozygous955091223
5135664804135664805CT22GENIChomozygous955091224
5135665105135665106GT20GENIChomozygous955091225
5135666369135666370CT18GENIChomozygous955091226
5135668452135668453TC36GENIChomozygous955091227
5135668822135668823GA32GENIChomozygous955091228
5135669568135669569AG25GENIChomozygous955091229
5135669593135669594GA28GENIChomozygous955091230
5135669628135669629TC29GENIChomozygous955091231
5135669823135669824TC31GENIChomozygous955091232
5135669857135669858AC30GENIChomozygous955091233
5135672173135672174TC37GENIChomozygous955091234
5135672864135672865TC31GENIChomozygous955091235
5135673053135673054GA36GENICpossibly homozygous955091236
5135673187135673188AG34GENIChomozygous955091237
5135673910135673911AG33GENIChomozygous955091238
5135673963135673964CT35GENIChomozygous955091239
5135674186135674187GA32GENIChomozygous955091240
5135674254135674255AG25GENIChomozygous955091241
5135674298135674299CT31GENIChomozygous955091242
5135674436135674437TC21GENIChomozygous955091243
5135674786135674787TC42GENIChomozygous955091244
5135674974135674975TC21GENIChomozygous955091245
5135675084135675085CT15GENIChomozygous955091246