| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:38252248-38252353 | Common:1; Rare:59 | ||||
| chr15:38454053-38454191 | Rare:55 | ||||
| chr15:39580864-39581083 | Rare:59 | ||||
| chr15:39782806-39782887 | Rare:21 | ||||
| chr15:39920252-39920327 | Rare:12 | ||||
| chr15:39933973-39934202 | Common:4; Rare:80 | ||||
| chr15:40039078-40039354 | Common:1; Rare:106 | ||||
| chr15:40160909-40161135 | Common:3; Rare:51 | ||||
| chr15:40405613-40405827 | Common:2; Rare:62; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr15:40569179-40569367 | Common:3; Rare:47 | ||||
| chr15:40593906-40594334 | Common:2; Rare:132 | ||||
| chr15:40695050-40695248 | Common:2; Rare:61 | ||||
| chr15:40755209-40755427 | Common:2; Rare:73 | ||||
| chr15:40807424-40807761 | Common:4; Rare:113 | ||||
| chr15:41115991-41116030 | Rare:15 |