| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127030544-127030768 | Common:2; Rare:52 | ||||
| chr5:127517495-127517712 | Common:7; Rare:95 | ||||
| chr5:131165177-131165407 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr5:131170693-131171013 | Common:1; Rare:68; Clinvar (benign):2 | ||||
| chr5:131635160-131635422 | Common:1; Rare:99 | ||||
| chr5:131796936-131797239 | Rare:87 | ||||
| chr5:132227797-132227929 | Common:2; Rare:33 | ||||
| chr5:132294138-132294411 | Common:1; Rare:67 | ||||
| chr5:132490761-132491020 | Rare:68 | ||||
| chr5:132737506-132737608 | Rare:31 | ||||
| chr5:132777188-132777351 | Common:1; Rare:39 | ||||
| chr5:132866402-132866711 | Common:2; Rare:101; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963281-132963580 | Common:3; Rare:68 | ||||
| chr5:133051819-133052355 | Common:1; Rare:172 | ||||
| chr5:133968570-133968731 | Rare:61 |