| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41283774-41284079 | Common:3; Rare:161 | ||||
| chr15:41495900-41496710 | Common:6; Rare:267 | ||||
| chr15:41568420-41568810 | Common:2; Rare:144 | ||||
| chr15:42392390-42392900 | Common:6; Rare:216; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):10 | ||||
| chr15:43814470-43815290 | Common:2; Rare:221 | ||||
| chr15:44979670-44980086 | Common:3; Rare:110 | ||||
| chr15:45279190-45279463 | Common:4; Rare:210 | ||||
| chr15:50766576-50766682 | Common:1; Rare:28 | ||||
| chr15:51037430-51038130 | Common:3; Rare:236 | ||||
| chr15:51094670-51095030 | Common:8; Rare:121 | ||||
| chr15:52008998-52009329 | Common:1; Rare:76 | ||||
| chr15:52288390-52288820 | Common:4; Rare:110 | ||||
| chr15:53453450-53454010 | Common:3; Rare:98 | ||||
| chr15:53710919-53711148 | Rare:129 | ||||
| chr15:53831066-53831392 | Common:7; Rare:133 |