| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:58428359-58428453 | Rare:27; Clinvar (benign):2 | ||||
| chr14:59188376-59188777 | Common:3; Rare:114 | ||||
| chr14:59188888-59189135 | Common:1; Rare:54 | ||||
| chr14:59354729-59354938 | Common:2; Rare:32 | ||||
| chr14:59361602-59361803 | Rare:34 | ||||
| chr14:59483416-59483450 | Rare:8 | ||||
| chr14:59483452-59483700 | Common:4; Rare:48 | ||||
| chr14:59870479-59870623 | Common:1; Rare:48 | ||||
| chr14:59870683-59870966 | Common:2; Rare:67 | ||||
| chr14:60091129-60091460 | Common:2; Rare:75 | ||||
| chr14:60091599-60091620 | Rare:5 | ||||
| chr14:60091633-60092482 | Common:10; Rare:289 | ||||
| chr14:60092661-60092697 | Rare:8 | ||||
| chr14:60164796-60165564 | Common:3; Rare:228 | ||||
| chr14:60248836-60249326 | Common:6; Rare:161 |