chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134173993341739934AG44GENIChomozygous114541096
134174055441740555TC44GENIChomozygous114329878
134174100041741001TC53GENIChomozygous114329880
134174230841742309GA23GENIChomozygous114329882
134174320341743204AG50GENIChomozygous114329884
134174359441743595CT59GENIChomozygous114329886
134174723341747234CT60GENIChomozygous114329888
134174730541747306TC46GENICpossibly homozygous114329890
134174776141747762CT42GENIChomozygous114329892
134174842841748429CA35GENIChomozygous114329894
134174968041749681GA39GENIChomozygous114329896
134175002841750029TC36GENIChomozygous114329898
134175190641751907AC52GENIChomozygous114329900
134175235441752355GT48GENIChomozygous114329902
134175523741755237A37GENIChomozygous129046429
134174319841743200TA48GENIChomozygous129046425
134175020941750224CTGACTAATTCAGTA41GENIChomozygous129046427
134174988741749888CT34GENIChomozygous114821367
134175316941753169G39GENIChomozygous129046428
134175543141755432TA39GENIChomozygous114329904
134175873041758731CT53GENIChomozygous114329906
134175885041758851GA46GENIChomozygous114329908
134175891141758912GC39GENIChomozygous114329910