| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74540956-74541276 | Common:4; Rare:110 | ||||
| chr15:74598381-74598506 | Common:1; Rare:50 | ||||
| chr15:74615733-74615891 | Common:2; Rare:51 | ||||
| chr15:74889800-74890076 | Rare:79; Clinvar (pathogenic):1 | ||||
| chr15:74937987-74938247 | Common:2; Rare:91 | ||||
| chr15:74995418-74995631 | Common:6; Rare:91 | ||||
| chr15:75023457-75023609 | Common:1; Rare:32 | ||||
| chr15:75335988-75336092 | Common:1; Rare:49 | ||||
| chr15:75347531-75347822 | Common:2; Rare:67 | ||||
| chr15:75368585-75368709 | Rare:37 | ||||
| chr15:75625612-75625894 | Common:2; Rare:64 | ||||
| chr15:75640166-75640428 | Common:1; Rare:89 | ||||
| chr15:76905318-76905489 | Common:1; Rare:64 | ||||
| chr15:77420085-77420467 | Common:2; Rare:112 | ||||
| chr15:78149176-78149406 | Common:1; Rare:75 |