chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37676577676765777GA28GENIChomozygous136754936
37676581476765815AG29GENIChomozygous136754937
37676709576767095CA12GENIChomozygous136574128
37676714476767145TC17GENIChomozygous136754938
37676806376768064TC28GENIChomozygous136754939
37676933376769334CA15GENIChomozygous136754940
37676952476769525GA18GENIChomozygous136754941
37676986776769868CT20GENIChomozygous136754942
37677052476770529TTTTG17GENIChomozygous136574129
37677063076770631TC22GENIChomozygous136754943
37677066076770661CT24GENIChomozygous136754944
37677214676772147GT14GENIChomozygous136754945
37677545376775453C24GENIChomozygous136574130
37677553776775541TTGT17GENIChomozygous136574131
37677661376776614GA20GENIChomozygous136754946
37677982976779830GA14GENIChomozygous136754947
37678002776780027CATA19GENIChomozygous136574132
37678338876783388TGTT14GENIChomozygous136574133
37678383676783837GA20GENIChomozygous136754948
37678547476785475CT13GENIChomozygous136754949
37678679976786800AG16GENIChomozygous136754950
37678712576787126CT17GENIChomozygous136754951
37679751876797519AC10GENIChomozygous136754956
37678932276789323GA13GENICpossibly homozygous136754952
37679129676791297GT22GENIChomozygous136754953
37679650076796501GC18GENIChomozygous136754954
37679677276796773GT15GENIChomozygous136754955
37678932276789323G13GENICheterozygous403068891
37679780976797810GA17GENIChomozygous136754957
37679852576798526CT16GENIChomozygous136754958
37679882076798821GA14GENIChomozygous136754959
37679887176798872TC17GENIChomozygous136754960
37679966676799667GA21GENIChomozygous136754961
37679991376799914GA18GENIChomozygous136754962