| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40039064-40039329 | Rare:107 | ||||
| chr15:40106589-40106787 | Rare:32 | ||||
| chr15:40108074-40108212 | Rare:32 | ||||
| chr15:40108827-40109244 | Common:1; Rare:103 | ||||
| chr15:40160888-40161185 | Common:4; Rare:68 | ||||
| chr15:40161190-40161365 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:40161389-40161505 | Rare:24 | ||||
| chr15:40239108-40239239 | Common:1; Rare:23 | ||||
| chr15:40239345-40239515 | Common:1; Rare:31 | ||||
| chr15:40252826-40252931 | Common:1; Rare:30 | ||||
| chr15:40252998-40253062 | Rare:18 | ||||
| chr15:40253133-40253148 | Rare:3 | ||||
| chr15:40291254-40291484 | Common:3; Rare:74 | ||||
| chr15:40340304-40340385 | Rare:10 | ||||
| chr15:40340899-40341021 | Common:1; Rare:45 |