chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
142270692222706923TG3GENIChomozygous118683729
142270696922706970GA10GENIChomozygous118683730
142270697122706972CG10GENIChomozygous118683731
142270697622706977CT10GENIChomozygous118683732
142270698022706981TC10GENIChomozygous118683733
142270699822706999TC11GENIChomozygous118683734
142270700122707002CA11GENIChomozygous118683735
142270700622707007GC11GENIChomozygous118683736
142270703122707032GT14GENIChomozygous123872478
142270709422707095TC13GENIChomozygous118683737
142270712122707122AG16GENIChomozygous118683738
142270713422707135GA17GENIChomozygous118683739
142270723422707235TC11GENIChomozygous118683740
142270727822707279TG8GENIChomozygous118683741
142270731822707319AG6GENIChomozygous118683742
142270733222707333GA6GENIChomozygous118683743
142270734022707341GA7GENIChomozygous118683744
142270740922707410GA9GENIChomozygous118794513
142270741822707419CT9GENIChomozygous118794514
142270743522707436TG9GENICpossibly homozygous118794515
142270751722707518CT4GENIChomozygous129205389
142270703022707030T14GENIChomozygous129133967
142270749922707500A5GENIChomozygous129133968
142270735422707355GA8GENIChomozygous118780815
142270736822707369AG8GENIChomozygous118780816
142270750022707501CG5GENIChomozygous129205388