| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:39782794-39782899 | Rare:28 | ||||
| chr15:39933960-39934230 | Common:4; Rare:99 | ||||
| chr15:40038838-40039362 | Common:2; Rare:183 | ||||
| chr15:40252356-40252664 | Common:1; Rare:116 | ||||
| chr15:40340238-40340397 | Rare:27 | ||||
| chr15:40405632-40405830 | Common:2; Rare:60; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr15:40569192-40569374 | Common:3; Rare:47 | ||||
| chr15:40695050-40695227 | Common:2; Rare:53 | ||||
| chr15:40755214-40755367 | Common:1; Rare:50 | ||||
| chr15:40763928-40764119 | Rare:48 | ||||
| chr15:40807057-40807106 | Rare:13 | ||||
| chr15:40807436-40807761 | Common:4; Rare:107 | ||||
| chr15:40873708-40873865 | Rare:44 | ||||
| chr15:40894370-40894555 | Rare:53 | ||||
| chr15:40953222-40953479 | Common:2; Rare:69 |