| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138033039-138033195 | Common:1; Rare:58 | ||||
| chr5:138178941-138179178 | Common:3; Rare:50 | ||||
| chr5:138331792-138332122 | Common:1; Rare:80 | ||||
| chr5:138337995-138338307 | Common:2; Rare:131 | ||||
| chr5:138465634-138466078 | Common:1; Rare:179 | ||||
| chr5:138543058-138543499 | Common:3; Rare:126 | ||||
| chr5:138543696-138543770 | Rare:18 | ||||
| chr5:138575668-138575951 | Rare:80 | ||||
| chr5:138753255-138753507 | Common:2; Rare:87 | ||||
| chr5:139198263-139198555 | Rare:93; Clinvar (benign):1 | ||||
| chr5:139293918-139294012 | Rare:25 | ||||
| chr5:139341572-139341929 | Common:1; Rare:89 | ||||
| chr5:139404029-139404358 | Common:2; Rare:89 | ||||
| chr5:139439453-139439646 | Common:2; Rare:52 | ||||
| chr5:139561100-139561405 | Common:1; Rare:121 |