| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40763832-40764124 | Common:4; Rare:132 | ||||
| chr15:40807036-40807149 | Rare:57 | ||||
| chr15:40807394-40807797 | Common:8; Rare:253 | ||||
| chr15:40894171-40894555 | Rare:194 | ||||
| chr15:41115590-41115910 | Rare:122 | ||||
| chr15:41115959-41116084 | Rare:64 | ||||
| chr15:41116127-41116306 | Common:4; Rare:88 | ||||
| chr15:41116371-41116770 | Common:2; Rare:215 | ||||
| chr15:41230630-41230940 | Common:1; Rare:86 | ||||
| chr15:41231121-41231347 | Rare:78 | ||||
| chr15:41402360-41402584 | Common:8; Rare:123; Clinvar:3; Clinvar (benign):2 | ||||
| chr15:41416934-41417196 | Common:8; Rare:223 | ||||
| chr15:41493090-41493370 | Rare:107 | ||||
| chr15:41493727-41493923 | Rare:65 | ||||
| chr15:41494300-41494600 | Rare:128 |