chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69159674891596749GC5GENICheterozygous115138346
69159716591597166AG6GENIChomozygous115138347
69159776491597765AG10GENIChomozygous114898727
69159870891598709GA10GENIChomozygous114898729
69160072191600722AG12GENIChomozygous114898733
69160363791603638CT16GENIChomozygous115138349
69160505991605060GT13GENIChomozygous115138350
69160555291605553TA5GENIChomozygous114898741
69160820191608202GA10GENIChomozygous115138351
69160851991608520GC6GENIChomozygous115138353
69160859991608600AG7GENIChomozygous114898761
69161139891611399GT11GENIChomozygous114898769
69161264691612647TC6GENIChomozygous114898771
69161370491613705CT8GENIChomozygous114898773
69161800191618002CT13GENIChomozygous115138355
69161843391618434TA6GENIChomozygous114898779
69161995791619958CA3GENIChomozygous115138356
69162033591620336GA4GENIChomozygous114898781
69162218291622183AG9GENIChomozygous114898783
69162397891623979AG11GENIChomozygous114898785
69162462191624622CT9GENIChomozygous114898795
69162505191625052AG6GENIChomozygous114898797
69162724391627244AT12GENIChomozygous114898799
69162724991627250AT13GENIChomozygous114898801
69162753091627531TG6GENIChomozygous115138358
69162822791628228TG14GENIChomozygous114898805