| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:132369628-132369759 | Common:2; Rare:37 | ||||
| chr5:132410603-132410984 | Common:1; Rare:78 | ||||
| chr5:132490770-132491020 | Rare:64 | ||||
| chr5:132556813-132557020 | Common:1; Rare:70; Clinvar:1 | ||||
| chr5:132830642-132830724 | Rare:25 | ||||
| chr5:132866471-132866692 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132963499-132963746 | Rare:67 | ||||
| chr5:133051857-133052344 | Common:1; Rare:155 | ||||
| chr5:133968542-133968688 | Rare:69 | ||||
| chr5:134004510-134004861 | Common:2; Rare:122 | ||||
| chr5:134004894-134005309 | Rare:101 | ||||
| chr5:134226015-134226407 | Common:1; Rare:126 | ||||
| chr5:134371027-134371184 | Common:1; Rare:40 | ||||
| chr5:134371301-134371597 | Common:4; Rare:120 | ||||
| chr5:134411852-134411990 | Rare:43 |