| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131263876-131264133 | Common:2; Rare:97 | ||||
| chr5:131635043-131635430 | Common:1; Rare:134 | ||||
| chr5:131796922-131797208 | Rare:83 | ||||
| chr5:132294111-132294441 | Common:1; Rare:78 | ||||
| chr5:132369538-132369977 | Common:9; Rare:144; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:132370173-132370374 | Common:2; Rare:79; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):6 | ||||
| chr5:132410603-132410991 | Common:1; Rare:78 | ||||
| chr5:132489463-132489589 | Rare:27 | ||||
| chr5:132490711-132491108 | Common:2; Rare:105 | ||||
| chr5:132556892-132557220 | Rare:121; Clinvar:1 | ||||
| chr5:132830228-132830351 | Rare:23 | ||||
| chr5:132830605-132830794 | Rare:53 | ||||
| chr5:132866471-132866713 | Common:2; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963260-132963403 | Rare:32 | ||||
| chr5:132963489-132963742 | Rare:68 |