| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:44962728-44962973 | Rare:63 | ||||
| chr14:45083877-45084277 | Common:3; Rare:229 | ||||
| chr14:45134133-45134273 | Common:2; Rare:77 | ||||
| chr14:45134328-45134790 | Rare:165 | ||||
| chr14:45135714-45136041 | Common:3; Rare:202 | ||||
| chr14:45136128-45136257 | Rare:47; Clinvar:3 | ||||
| chr14:45253004-45253702 | Common:8; Rare:559 | ||||
| chr14:45253878-45254380 | Rare:203 | ||||
| chr14:47626335-47626439 | Rare:30 | ||||
| chr14:47626550-47626689 | Common:2; Rare:60 | ||||
| chr14:47626760-47627310 | Common:8; Rare:149 | ||||
| chr14:47675267-47675420 | Common:3; Rare:24 | ||||
| chr14:49586294-49586822 | Common:3; Rare:508; Clinvar (benign):2 | ||||
| chr14:49598515-49599382 | Common:12; Rare:766 | ||||
| chr14:49620536-49620887 | Common:6; Rare:370; Clinvar:12 |