| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74461106-74461323 | Rare:66 | ||||
| chr15:74540946-74541283 | Common:4; Rare:115 | ||||
| chr15:74781869-74782091 | Common:3; Rare:69 | ||||
| chr15:74843106-74843339 | Common:1; Rare:66 | ||||
| chr15:74872978-74873109 | Rare:28 | ||||
| chr15:74889987-74890089 | Rare:48; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74937966-74938262 | Common:2; Rare:97 | ||||
| chr15:75347535-75347865 | Common:2; Rare:82 | ||||
| chr15:75451677-75451985 | Common:1; Rare:83 | ||||
| chr15:75625591-75625826 | Common:2; Rare:58 | ||||
| chr15:76059754-76059963 | Common:1; Rare:71 | ||||
| chr15:77420081-77420487 | Common:2; Rare:122 | ||||
| chr15:78131213-78131509 | Common:4; Rare:76; Clinvar (benign):2 | ||||
| chr15:78149161-78149420 | Common:1; Rare:89 | ||||
| chr15:78265932-78266218 | Common:1; Rare:53 |