| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:58245387-58245424 | Common:1; Rare:10 | ||||
| chr14:58297725-58298001 | Common:1; Rare:79 | ||||
| chr14:58298031-58298639 | Rare:166 | ||||
| chr14:58299896-58300029 | Common:1; Rare:24 | ||||
| chr14:58331194-58331429 | Common:1; Rare:48 | ||||
| chr14:58395765-58395953 | Rare:58 | ||||
| chr14:58395987-58396109 | Rare:39 | ||||
| chr14:58426883-58426945 | Rare:19 | ||||
| chr14:58427011-58427096 | Common:2; Rare:12 | ||||
| chr14:58427130-58427547 | Rare:99 | ||||
| chr14:58427589-58427834 | Rare:79 | ||||
| chr14:58427954-58428037 | Rare:21 | ||||
| chr14:58428376-58428451 | Rare:22; Clinvar (benign):1 | ||||
| chr14:58637502-58637695 | Common:1; Rare:51 | ||||
| chr14:58638056-58638211 | Rare:41 |