| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132490771-132491043 | Rare:70 | ||||
| chr5:132556838-132557012 | Common:1; Rare:61; Clinvar:1 | ||||
| chr5:132866318-132866713 | Common:2; Rare:122; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963509-132963840 | Common:1; Rare:81 | ||||
| chr5:133051851-133052344 | Common:1; Rare:159 | ||||
| chr5:133968560-133968708 | Rare:67 | ||||
| chr5:134004651-134004851 | Common:1; Rare:74 | ||||
| chr5:134004875-134004985 | Rare:28 | ||||
| chr5:134226022-134226407 | Common:1; Rare:124 | ||||
| chr5:134371015-134371184 | Common:1; Rare:47 | ||||
| chr5:134371393-134371618 | Common:3; Rare:101 | ||||
| chr5:134411850-134412008 | Rare:53 | ||||
| chr5:134632762-134632929 | Rare:33 | ||||
| chr5:134648715-134648848 | Rare:35 | ||||
| chr5:134738353-134738616 | Rare:100 |