| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138033073-138033175 | Common:1; Rare:35 | ||||
| chr5:138178604-138178724 | Rare:30 | ||||
| chr5:138178946-138179186 | Common:3; Rare:48 | ||||
| chr5:138331783-138332130 | Common:2; Rare:85 | ||||
| chr5:138337995-138338283 | Common:1; Rare:112 | ||||
| chr5:138543095-138543446 | Common:2; Rare:106 | ||||
| chr5:138753261-138753507 | Common:2; Rare:85 | ||||
| chr5:139198280-139198526 | Rare:82; Clinvar (benign):1 | ||||
| chr5:139273978-139274142 | Rare:76 | ||||
| chr5:139341700-139341953 | Common:1; Rare:66 | ||||
| chr5:139404050-139404232 | Rare:64 | ||||
| chr5:139482282-139482392 | Rare:17 | ||||
| chr5:139561100-139561393 | Common:1; Rare:117 | ||||
| chr5:139561724-139561807 | Rare:35 | ||||
| chr5:140175017-140175268 | Common:1; Rare:62 |