chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109496962994969630CT21GENIChomozygous116827029
109497000394970004TA19GENIChomozygous116827031
109497025294970253TC19GENIChomozygous116827033
109497034394970344CT8GENIChomozygous116955665
109497112894971129GT13GENICheterozygous126435673
109497116294971163CT21GENICpossibly homozygous126435675
109497268594972686TC12GENIChomozygous116955667
109497406694974067CG16GENIChomozygous116955671
109497427694974277GA6GENIChomozygous116955673
109497487194974872TC25GENIChomozygous116955675
109497635994976360GA23GENIChomozygous116955676
109497647294976473CG24GENIChomozygous116955677