| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74624486-74624789 | Rare:49 | ||||
| chr15:74627228-74627580 | Common:3; Rare:83 | ||||
| chr15:74695946-74696093 | Rare:51 | ||||
| chr15:74843087-74843318 | Common:2; Rare:74 | ||||
| chr15:74889731-74890076 | Rare:93; Clinvar (pathogenic):1 | ||||
| chr15:74906787-74906871 | Rare:39 | ||||
| chr15:74937961-74938265 | Common:2; Rare:97 | ||||
| chr15:74956767-74956873 | Common:1; Rare:43 | ||||
| chr15:74995394-74995652 | Common:7; Rare:105 | ||||
| chr15:75201758-75201924 | Common:1; Rare:59 | ||||
| chr15:75335973-75336089 | Common:1; Rare:51 | ||||
| chr15:75347525-75347905 | Common:2; Rare:95 | ||||
| chr15:75351923-75352159 | Rare:82 | ||||
| chr15:75362341-75362707 | Common:1; Rare:120 | ||||
| chr15:75368189-75368225 | Rare:14 |