chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8116754706116754707AG27GENIChomozygous116670085
8116754997116754998AG32GENIChomozygous116670087
8116755050116755051GA33GENIChomozygous116670089
8116755513116755514TC36GENIChomozygous116670091
8116756428116756429GA45GENIChomozygous116670093
8116757060116757061GA34GENIChomozygous116670097
8116757826116757827AG26GENIChomozygous116670099
8116758149116758150CA40GENIChomozygous116670101
8116758241116758242CT29GENIChomozygous116670103
8116758394116758395AG29GENIChomozygous116670105
8116759732116759733TC56GENIChomozygous116670107
8116760455116760456CA39GENIChomozygous116670109
8116760705116760706CT31GENIChomozygous116670111
8116761477116761478CG28GENICpossibly homozygous116670113
8116761537116761538GA31GENIChomozygous116670115
8116762690116762691AT40GENIChomozygous116670117
8116762838116762839CT37GENIChomozygous116670119
8116764707116764708CG30GENIChomozygous116670121
8116765051116765052CT28GENIChomozygous116670123