| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:27424837-27425011 | Common:1; Rare:51 | ||||
| chr13:27425904-27426129 | Rare:41 | ||||
| chr13:27449915-27450745 | Common:7; Rare:278 | ||||
| chr13:27450993-27451452 | Common:4; Rare:97 | ||||
| chr13:27619941-27620042 | Common:1; Rare:21 | ||||
| chr13:27620056-27620164 | Rare:28 | ||||
| chr13:27620261-27621037 | Common:6; Rare:252 | ||||
| chr13:27621288-27621504 | Common:2; Rare:54 | ||||
| chr13:27621616-27621993 | Common:7; Rare:158; Clinvar:6; Clinvar (benign):6 | ||||
| chr13:27919816-27920015 | Common:1; Rare:54 | ||||
| chr13:28138049-28138307 | Common:2; Rare:80 | ||||
| chr13:28138342-28138738 | Common:7; Rare:112 | ||||
| chr13:28138786-28138859 | Rare:11 | ||||
| chr13:28138895-28139223 | Common:1; Rare:92 | ||||
| chr13:28139226-28139515 | Common:1; Rare:67 |