| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70097839-70098092 | Common:1; Rare:59 | ||||
| chr15:70687553-70687805 | Rare:82 | ||||
| chr15:70763367-70763840 | Common:2; Rare:148 | ||||
| chr15:70853205-70853440 | Common:1; Rare:40 | ||||
| chr15:70892352-70892887 | Common:1; Rare:131 | ||||
| chr15:71115275-71115488 | Rare:45 | ||||
| chr15:72118033-72118467 | Common:3; Rare:148 | ||||
| chr15:72231086-72231520 | Common:3; Rare:135 | ||||
| chr15:72375951-72376073 | Common:2; Rare:55; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
| chr15:72474174-72474404 | Rare:87 | ||||
| chr15:72474618-72474777 | Common:1; Rare:42 | ||||
| chr15:72474874-72474945 | Rare:29 | ||||
| chr15:72686147-72686234 | Common:2; Rare:35; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:72731435-72731712 | Common:1; Rare:81; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr15:72783662-72783866 | Common:2; Rare:93 |