| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40874164-40874352 | Common:2; Rare:48 | ||||
| chr15:40894178-40894597 | Rare:109 | ||||
| chr15:40894896-40895160 | Rare:41 | ||||
| chr15:40929132-40929375 | Common:1; Rare:58 | ||||
| chr15:40952758-40953086 | Rare:71 | ||||
| chr15:40953088-40953536 | Common:4; Rare:130 | ||||
| chr15:41115625-41115797 | Rare:44 | ||||
| chr15:41115807-41116310 | Common:2; Rare:138 | ||||
| chr15:41116332-41116880 | Common:1; Rare:163 | ||||
| chr15:41230650-41230876 | Rare:67 | ||||
| chr15:41231049-41231378 | Rare:105 | ||||
| chr15:41231388-41231463 | Rare:21; Clinvar (pathogenic):1 | ||||
| chr15:41231616-41231805 | Rare:41 | ||||
| chr15:41332110-41332369 | Common:1; Rare:87 | ||||
| chr15:41332520-41333054 | Common:2; Rare:209 |