chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
37676577676765777GA58GENIChomozygous136754936
37676581476765815AG56GENIChomozygous136754937
37676709576767095CA27GENIChomozygous136574128
37676714476767145TC33GENIChomozygous136754938
37676806376768064TC42GENIChomozygous136754939
37676768376767684CG5GENICheterozygous403068885
37676768376767684C5GENICheterozygous403068886
37676933376769334CA48GENIChomozygous136754940
37676952476769525GA34GENIChomozygous136754941
37676986776769868CT52GENIChomozygous136754942
37677052476770529TTTTG42GENIChomozygous136574129
37677063076770631TC35GENIChomozygous136754943
37677066076770661CT29GENIChomozygous136754944
37677214676772147GT44GENIChomozygous136754945
37677545376775453C45GENIChomozygous136574130
37677553776775541TTGT36GENIChomozygous136574131
37677661376776614GA35GENIChomozygous136754946
37677982976779830GA40GENIChomozygous136754947
37678002776780027CATA43GENIChomozygous136574132
37678338876783388TGTT37GENIChomozygous136574133
37678383676783837GA51GENIChomozygous136754948
37678547476785475CT51GENIChomozygous136754949
37678679976786800AG54GENIChomozygous136754950
37678712576787126CT54GENIChomozygous136754951
37678932276789323GA36GENICpossibly homozygous136754952
37678932276789323G36GENICheterozygous403068891
37679129676791297GT43GENIChomozygous136754953
37679650076796501GC49GENIChomozygous136754954
37679677276796773GT42GENIChomozygous136754955
37679751876797519AC52GENIChomozygous136754956
37679780976797810GA50GENIChomozygous136754957
37679852576798526CT51GENIChomozygous136754958
37679882076798821GA53GENIChomozygous136754959
37679887176798872TC55GENIChomozygous136754960
37679966676799667GA44GENIChomozygous136754961
37679991376799914GA40GENIChomozygous136754962