| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74540915-74541358 | Common:6; Rare:156 | ||||
| chr15:74541666-74541744 | Rare:20 | ||||
| chr15:74615559-74615901 | Common:4; Rare:108 | ||||
| chr15:74695948-74696055 | Rare:38 | ||||
| chr15:74781916-74782129 | Common:3; Rare:71 | ||||
| chr15:74843130-74843338 | Common:1; Rare:54 | ||||
| chr15:74873303-74873423 | Common:2; Rare:29 | ||||
| chr15:74889962-74890085 | Rare:54; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74906700-74906872 | Common:2; Rare:63 | ||||
| chr15:74937952-74938247 | Common:2; Rare:95 | ||||
| chr15:74956718-74956870 | Common:1; Rare:67 | ||||
| chr15:74956987-74957222 | Common:1; Rare:66 | ||||
| chr15:74995359-74995671 | Common:7; Rare:115 | ||||
| chr15:75347001-75347109 | Rare:21 | ||||
| chr15:75368528-75368632 | Rare:56 |