chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37676577676765777GA23GENICpossibly homozygous136754936
37676581476765815AG30GENIChomozygous136754937
37676714476767145TC16GENIChomozygous136754938
37676768576767686CG11GENICheterozygous403068887
37676768576767686C11GENICheterozygous403068888
37676768776767688CG11GENICheterozygous403068889
37676768776767688C11GENICheterozygous403068890
37676806376768064TC31GENIChomozygous136754939
37676933376769334CA20GENIChomozygous136754940
37676952476769525GA38GENIChomozygous136754941
37676986776769868CT19GENIChomozygous136754942
37677063076770631TC22GENIChomozygous136754943
37677066076770661CT21GENIChomozygous136754944
37677214676772147GT17GENIChomozygous136754945
37677545376775453C22GENIChomozygous136574130
37676709576767095CA13GENIChomozygous136574128
37677052476770529TTTTG20GENICpossibly homozygous136574129
37677553776775541TTGT16GENIChomozygous136574131
37677661376776614GA22GENIChomozygous136754946
37677982976779830GA20GENIChomozygous136754947
37678002776780027CATA30GENIChomozygous136574132
37678338876783388TGTT15GENIChomozygous136574133
37678383676783837GA24GENIChomozygous136754948
37678547476785475CT19GENIChomozygous136754949
37678679976786800AG19GENIChomozygous136754950
37678712576787126CT22GENIChomozygous136754951
37678932276789323GA31GENICpossibly homozygous136754952
37678932276789323G31GENICheterozygous403068891
37679129676791297GT22GENIChomozygous136754953
37679650076796501GC28GENIChomozygous136754954
37679677276796773GT24GENIChomozygous136754955
37679751876797519AC17GENIChomozygous136754956
37679780976797810GA24GENIChomozygous136754957
37679852576798526CT27GENIChomozygous136754958
37679882076798821GA26GENIChomozygous136754959
37679887176798872TC25GENIChomozygous136754960
37679966676799667GA29GENIChomozygous136754961
37679991376799914GA32GENIChomozygous136754962