chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4136805806136805807GA8GENIChomozygous56941979
4136810329136810330TTTG10GENICpossibly homozygous56941980
4136811341136811342GA21GENIChomozygous56941981
4136811464136811465GA32GENIChomozygous56941982
4136811845136811846GC20GENIChomozygous56941983
4136813066136813067AG19GENIChomozygous56941984
4136813105136813106GA18GENIChomozygous56941985
4136813281136813282CCAAAA12GENIChomozygous58338893
4136813513136813514TC20GENIChomozygous56941987
4136815701136815702CT21GENIChomozygous56941988
4136816599136816600TG26GENIChomozygous56941989
4136818347136818348AG12GENIChomozygous56941990
4136818667136818668TTCTCTCTCTCTCTCTCTCTC12GENICheterozygous58338895