| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:89334787-89335069 | Common:3; Rare:107 | ||||
| chr15:89690660-89690773 | Common:1; Rare:38 | ||||
| chr15:89690782-89690812 | Rare:6 | ||||
| chr15:89776561-89776655 | Rare:47; Clinvar:1; Clinvar (pathogenic):4 | ||||
| chr15:89893939-89894035 | Rare:36 | ||||
| chr15:89912815-89913015 | Common:2; Rare:68 | ||||
| chr15:90001241-90001325 | Common:1; Rare:17 | ||||
| chr15:90184802-90184976 | Common:2; Rare:43 | ||||
| chr15:90221413-90221642 | Common:1; Rare:76 | ||||
| chr15:90233811-90234290 | Common:6; Rare:137 | ||||
| chr15:90265632-90266258 | Common:7; Rare:212 | ||||
| chr15:90352107-90352389 | Common:5; Rare:72 | ||||
| chr15:90387956-90388371 | Common:5; Rare:163 | ||||
| chr15:90483954-90484352 | Rare:92 | ||||
| chr15:90529815-90530153 | Common:4; Rare:108 |