| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:140114638-140115042 | Rare:80; Clinvar (benign):6 | ||||
| chr5:140175869-140176015 | Rare:26 | ||||
| chr5:140181069-140181185 | Common:1; Rare:17 | ||||
| chr5:140357758-140357903 | Common:1; Rare:29 | ||||
| chr5:140400150-140400431 | Rare:46 | ||||
| chr5:140400633-140400741 | Rare:21 | ||||
| chr5:140400766-140401283 | Common:1; Rare:118 | ||||
| chr5:140402780-140402876 | Rare:28 | ||||
| chr5:140555946-140556281 | Rare:60 | ||||
| chr5:140569369-140569629 | Common:1; Rare:57 | ||||
| chr5:140665427-140665470 | Common:1; Rare:12 | ||||
| chr5:140672615-140672901 | Common:9; Rare:74 | ||||
| chr5:140711126-140711291 | Common:1; Rare:49 | ||||
| chr5:140718788-140718926 | Common:4; Rare:48 | ||||
| chr5:140725968-140726321 | Common:3; Rare:85 |