chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69159776491597765AG16GENIChomozygous114898727
69159870891598709GA4GENICheterozygous114898729
69160010491600105TG22GENIChomozygous114898731
69160072191600722AG7GENIChomozygous114898733
69160108791601088AG6GENIChomozygous114898735
69160363791603638CT10GENIChomozygous115138349
69160505991605060GT26GENIChomozygous115138350
69160555291605553TA9GENIChomozygous114898741
69160820191608202GA20GENIChomozygous115138351
69160851991608520GC13GENIChomozygous115138353
69160859991608600AG6GENIChomozygous114898761
69161139891611399GT10GENIChomozygous114898769
69161264691612647TC25GENIChomozygous114898771
69161370491613705CT20GENIChomozygous114898773
69161651891616519TC5GENIChomozygous114898777
69161800191618002CT21GENIChomozygous115138355
69161843391618434TA7GENIChomozygous114898779
69161957891619579GC19GENIChomozygous126357997
69161976391619764GC8GENIChomozygous126372208
69161977991619780GC6GENIChomozygous126372209
69161995791619958CA20GENIChomozygous115138356
69162033591620336GA21GENIChomozygous114898781
69162218291622183AG17GENIChomozygous114898783
69162397891623979AG19GENIChomozygous114898785
69162462191624622CT13GENIChomozygous114898795
69162505191625052AG11GENIChomozygous114898797
69162753091627531TG17GENIChomozygous115138358
69162822791628228TG17GENIChomozygous114898805