| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40382833-40383043 | Common:1; Rare:103 | ||||
| chr15:40569192-40569366 | Common:3; Rare:42 | ||||
| chr15:40593906-40594035 | Common:1; Rare:58 | ||||
| chr15:40695058-40695198 | Rare:39 | ||||
| chr15:40763952-40764115 | Rare:39 | ||||
| chr15:40806862-40807152 | Common:5; Rare:63 | ||||
| chr15:40807415-40807776 | Common:4; Rare:123 | ||||
| chr15:40894210-40894477 | Rare:82 | ||||
| chr15:40929132-40929343 | Common:1; Rare:52 | ||||
| chr15:41115982-41116080 | Rare:30 | ||||
| chr15:41116566-41116688 | Rare:40 | ||||
| chr15:41402427-41402558 | Common:4; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:41416969-41417213 | Common:3; Rare:111 | ||||
| chr15:41621140-41621265 | Common:1; Rare:31 | ||||
| chr15:41660309-41660501 | Rare:65 |