| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23376857-23377051 | Rare:35 | ||||
| chr14:23555933-23556052 | Rare:32 | ||||
| chr14:23567468-23567573 | Rare:30 | ||||
| chr14:23567761-23567906 | Rare:31 | ||||
| chr14:23953661-23953813 | Common:6; Rare:53 | ||||
| chr14:24114998-24115292 | Common:2; Rare:81 | ||||
| chr14:24135943-24136248 | Rare:91 | ||||
| chr14:24141574-24141862 | Common:1; Rare:63 | ||||
| chr14:24146587-24146740 | Rare:53 | ||||
| chr14:24195597-24195696 | Rare:24 | ||||
| chr14:24213433-24213668 | Common:3; Rare:74 | ||||
| chr14:24232330-24232644 | Common:8; Rare:72 | ||||
| chr14:24242324-24242407 | Rare:29 | ||||
| chr14:24242571-24242741 | Common:1; Rare:35; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:24271491-24271606 | Common:1; Rare:27 |