| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131796970-131797231 | Rare:71 | ||||
| chr5:132369636-132369794 | Common:3; Rare:44; Clinvar (benign):1 | ||||
| chr5:132556795-132557012 | Common:1; Rare:73; Clinvar:1 | ||||
| chr5:132866470-132866694 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133051862-133052146 | Rare:100 | ||||
| chr5:133968582-133968737 | Rare:57 | ||||
| chr5:134004651-134004851 | Common:1; Rare:74 | ||||
| chr5:134225556-134225644 | Common:1; Rare:31 | ||||
| chr5:134371023-134371196 | Common:1; Rare:45 | ||||
| chr5:134371435-134371607 | Common:3; Rare:80 | ||||
| chr5:134411850-134411948 | Rare:37 | ||||
| chr5:134648662-134648840 | Rare:53 | ||||
| chr5:134874282-134874423 | Common:1; Rare:74 | ||||
| chr5:135399128-135399349 | Rare:58 | ||||
| chr5:138033012-138033175 | Common:1; Rare:59 |