| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132369595-132369759 | Common:3; Rare:48 | ||||
| chr5:132410603-132410951 | Common:1; Rare:67 | ||||
| chr5:132490764-132491015 | Rare:65 | ||||
| chr5:132866457-132866694 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963519-132963780 | Rare:68 | ||||
| chr5:133051862-133052216 | Rare:119 | ||||
| chr5:133968563-133968688 | Rare:61 | ||||
| chr5:134004504-134004838 | Common:2; Rare:113 | ||||
| chr5:134004894-134005040 | Rare:33 | ||||
| chr5:134176853-134177056 | Common:4; Rare:87 | ||||
| chr5:134225541-134225644 | Common:1; Rare:37 | ||||
| chr5:134225995-134226437 | Common:1; Rare:144 | ||||
| chr5:134371027-134371637 | Common:5; Rare:202 | ||||
| chr5:134411846-134412009 | Rare:56 | ||||
| chr5:134526152-134526219 | Rare:28 |