| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68229353-68229509 | Common:2; Rare:85; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:68229598-68230090 | Common:4; Rare:267; Clinvar:4; Clinvar (benign):8 | ||||
| chr15:68277645-68277879 | Common:8; Rare:100 | ||||
| chr15:68277933-68278124 | Rare:109 | ||||
| chr15:68817310-68817970 | Common:6; Rare:273 | ||||
| chr15:68818136-68818249 | Common:2; Rare:93 | ||||
| chr15:68818614-68819281 | Common:6; Rare:231 | ||||
| chr15:68820755-68821093 | Rare:204 | ||||
| chr15:69045630-69046200 | Common:2; Rare:165 | ||||
| chr15:69160342-69160694 | Common:7; Rare:197 | ||||
| chr15:69298761-69298986 | Common:6; Rare:87 | ||||
| chr15:69414161-69414465 | Rare:199 | ||||
| chr15:69452591-69452962 | Common:10; Rare:270 | ||||
| chr15:69452984-69453177 | Rare:111 | ||||
| chr15:70097807-70098112 | Common:12; Rare:145 |