| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132761160-132761351 | Rare:38 | ||||
| chr5:132830218-132830361 | Common:2; Rare:28 | ||||
| chr5:132830602-132830794 | Rare:53 | ||||
| chr5:132866467-132866694 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132873417-132873696 | Common:3; Rare:65 | ||||
| chr5:132963443-132963737 | Rare:82 | ||||
| chr5:133026533-133026777 | Common:5; Rare:55 | ||||
| chr5:133051862-133052268 | Rare:138 | ||||
| chr5:133968546-133968688 | Rare:69 | ||||
| chr5:134004647-134004911 | Common:1; Rare:97 | ||||
| chr5:134004923-134005079 | Rare:30 | ||||
| chr5:134225989-134226417 | Common:1; Rare:138 | ||||
| chr5:134226637-134226728 | Common:1; Rare:13 | ||||
| chr5:134371036-134371601 | Common:5; Rare:186 | ||||
| chr5:134411846-134412009 | Rare:56 |