Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:64465359-64465546 | Common:1; Rare:51 | ||||
chr14:64503607-64503887 | Common:2; Rare:107 | ||||
chr14:64504585-64504868 | Rare:85 | ||||
chr14:64914118-64914513 | Common:3; Rare:127 | ||||
chr14:64942734-64942754 | Rare:5 | ||||
chr14:64987086-64987278 | Rare:73 | ||||
chr14:65102237-65102804 | Common:9; Rare:167; Clinvar:5; Clinvar (benign):10 | ||||
chr14:66507813-66508167 | Rare:140 | ||||
chr14:66508379-66508557 | Rare:62; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:66509278-66509580 | Common:2; Rare:77 | ||||
chr14:67241117-67241565 | Common:1; Rare:114 | ||||
chr14:67359675-67360030 | Common:1; Rare:125 | ||||
chr14:67360247-67360381 | Common:2; Rare:37 | ||||
chr14:67619587-67619965 | Common:2; Rare:93 | ||||
chr14:67674622-67674933 | Common:1; Rare:73 |