| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40695034-40695227 | Common:2; Rare:61 | ||||
| chr15:40755198-40755435 | Common:3; Rare:80 | ||||
| chr15:40763944-40764120 | Rare:43 | ||||
| chr15:40807044-40807120 | Rare:20 | ||||
| chr15:40807382-40807911 | Common:6; Rare:168 | ||||
| chr15:40894361-40894477 | Rare:41 | ||||
| chr15:40953113-40953476 | Common:2; Rare:96 | ||||
| chr15:41115971-41116070 | Rare:31 | ||||
| chr15:41116566-41116708 | Rare:46 | ||||
| chr15:41230755-41230839 | Rare:18 | ||||
| chr15:41231049-41231373 | Rare:102 | ||||
| chr15:41402378-41402577 | Common:4; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:41416932-41417218 | Common:4; Rare:124 | ||||
| chr15:41544228-41544359 | Rare:54 | ||||
| chr15:41621176-41621275 | Common:1; Rare:30 |