| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138331660-138332140 | Common:4; Rare:222 | ||||
| chr5:138337717-138338293 | Common:6; Rare:302 | ||||
| chr5:138464900-138465370 | Common:3; Rare:198 | ||||
| chr5:138543045-138543591 | Common:5; Rare:290 | ||||
| chr5:138574780-138575290 | Common:5; Rare:142 | ||||
| chr5:138575284-138575961 | Common:4; Rare:433 | ||||
| chr5:138753252-138753507 | Common:4; Rare:147 | ||||
| chr5:139198209-139198556 | Rare:205; Clinvar (benign):2 | ||||
| chr5:139273975-139274213 | Rare:178 | ||||
| chr5:139293534-139294026 | Rare:239 | ||||
| chr5:139341584-139341924 | Common:1; Rare:87 | ||||
| chr5:139342230-139342620 | Common:9; Rare:237 | ||||
| chr5:139383276-139383441 | Rare:33 | ||||
| chr5:139404056-139404337 | Common:1; Rare:124 | ||||
| chr5:139439420-139439800 | Common:4; Rare:147 |