| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:128538202-128538388 | Common:5; Rare:60 | ||||
| chr5:129094474-129094787 | Common:3; Rare:135 | ||||
| chr5:131165098-131165389 | Common:3; Rare:107; Clinvar (benign):2 | ||||
| chr5:131170645-131171013 | Common:1; Rare:88; Clinvar (benign):2 | ||||
| chr5:131263911-131264109 | Rare:72 | ||||
| chr5:131635160-131635728 | Common:1; Rare:189 | ||||
| chr5:131796970-131797221 | Rare:68 | ||||
| chr5:132227793-132227900 | Common:2; Rare:27 | ||||
| chr5:132294111-132294441 | Common:1; Rare:78 | ||||
| chr5:132295327-132295434 | Rare:23 | ||||
| chr5:132369563-132369966 | Common:9; Rare:133; Clinvar:6; Clinvar (benign):6 | ||||
| chr5:132410601-132410951 | Common:1; Rare:67 | ||||
| chr5:132490754-132491020 | Rare:68 | ||||
| chr5:132556872-132557032 | Rare:60; Clinvar:1 | ||||
| chr5:132557150-132557283 | Rare:37 |