chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135664804135664805CT28GENIChomozygous798627699
5135665105135665106GT19GENICpossibly homozygous798627700
5135668452135668453TC31GENIChomozygous798627701
5135668822135668823GA24GENIChomozygous798627702
5135669118135669119TC50GENIChomozygous798627703
5135669568135669569AG30GENIChomozygous798627704
5135669593135669594GA32GENIChomozygous798627705
5135669628135669629TC33GENIChomozygous798627706
5135669823135669824TC24GENIChomozygous798627707
5135669857135669858AC24GENIChomozygous798627708
5135672173135672174TC40GENIChomozygous798627709
5135672497135672498CT26GENICpossibly homozygous798627710
5135672864135672865TC33GENIChomozygous798627711
5135673053135673054GA42GENIChomozygous798627712
5135673187135673188AG31GENIChomozygous798627713
5135673910135673911AG45GENIChomozygous798627714
5135673963135673964CT47GENIChomozygous798627715
5135674186135674187GA47GENIChomozygous798627716
5135674254135674255AG47GENIChomozygous798627717
5135674298135674299CT42GENIChomozygous798627718
5135674436135674437TC33GENIChomozygous798627719
5135674786135674787TC26GENIChomozygous798627720
5135674974135674975TC41GENIChomozygous798627721
5135675084135675085CT27GENIChomozygous798627722