chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135664103135664104GT15GENIChomozygous961044944
5135664105135664106GT13GENIChomozygous961044945
5135664804135664805CT16GENICpossibly homozygous961044946
5135666369135666370CT18GENIChomozygous961044947
5135668452135668453TC24GENIChomozygous961044948
5135668822135668823GA14GENIChomozygous961044949
5135669118135669119TC39GENIChomozygous961044950
5135669568135669569AG24GENIChomozygous961044951
5135669593135669594GA28GENIChomozygous961044952
5135669628135669629TC26GENIChomozygous961044953
5135669823135669824TC22GENIChomozygous961044954
5135669857135669858AC23GENIChomozygous961044955
5135672173135672174TC31GENIChomozygous961044956
5135672864135672865TC24GENIChomozygous961044957
5135673053135673054GA29GENIChomozygous961044958
5135673187135673188AG40GENIChomozygous961044959
5135673910135673911AG32GENIChomozygous961044960
5135673963135673964CT35GENIChomozygous961044961
5135674186135674187GA21GENIChomozygous961044962
5135674254135674255AG21GENIChomozygous961044963
5135674298135674299CT27GENIChomozygous961044964
5135674436135674437TC25GENIChomozygous961044965
5135674786135674787TC26GENICpossibly homozygous961044966
5135674974135674975TC22GENIChomozygous961044967
5135675084135675085CT18GENICpossibly homozygous961044968