chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69159674891596749GC16GENICpossibly homozygous115138346
69159716591597166AG20GENIChomozygous115138347
69159776491597765AG33GENIChomozygous114898727
69159992791599928TG21GENICheterozygous115503451
69159993091599931AG10GENICheterozygous118587360
69160010491600105TG7GENIChomozygous114898731
69160072191600722AG25GENIChomozygous114898733
69160363791603638CT20GENIChomozygous115138349
69160505991605060GT30GENIChomozygous115138350
69160555291605553TA31GENIChomozygous114898741
69160820191608202GA24GENIChomozygous115138351
69160851991608520GC15GENIChomozygous115138353
69160859991608600AG6GENIChomozygous114898761
69161139891611399GT23GENIChomozygous114898769
69161370491613705CT40GENIChomozygous114898773
69161800191618002CT34GENIChomozygous115138355
69161843391618434TA27GENIChomozygous114898779
69161995791619958CA23GENIChomozygous115138356
69162033591620336GA27GENIChomozygous114898781
69162218291622183AG25GENIChomozygous114898783
69162397891623979AG25GENIChomozygous114898785
69162462191624622CT32GENIChomozygous114898795
69162505191625052AG19GENIChomozygous114898797
69162724391627244AT17GENIChomozygous114898799
69162724991627250AT20GENIChomozygous114898801
69162753091627531TG26GENIChomozygous115138358
69162822791628228TG23GENIChomozygous114898805