| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74598370-74598535 | Common:1; Rare:70 | ||||
| chr15:74615559-74615891 | Common:4; Rare:106 | ||||
| chr15:74873275-74873447 | Common:5; Rare:58 | ||||
| chr15:74890005-74890076 | Rare:36; Clinvar (pathogenic):1 | ||||
| chr15:74937985-74938247 | Common:2; Rare:91 | ||||
| chr15:75347517-75347889 | Common:2; Rare:93 | ||||
| chr15:75368553-75368627 | Rare:35 | ||||
| chr15:75451677-75452032 | Common:1; Rare:94 | ||||
| chr15:75455790-75455884 | Rare:33 | ||||
| chr15:75625612-75625830 | Common:2; Rare:53 | ||||
| chr15:75640200-75640380 | Common:1; Rare:52 | ||||
| chr15:76059692-76059991 | Common:2; Rare:102 | ||||
| chr15:76292441-76292621 | Rare:74; Clinvar:1 | ||||
| chr15:77420057-77420467 | Common:2; Rare:118 | ||||
| chr15:77421101-77421333 | Common:1; Rare:59 |