| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131796928-131797265 | Rare:98 | ||||
| chr5:132227795-132228190 | Common:4; Rare:95 | ||||
| chr5:132410603-132410859 | Common:1; Rare:52 | ||||
| chr5:132490774-132491020 | Rare:64 | ||||
| chr5:132556829-132557024 | Common:1; Rare:71; Clinvar:1 | ||||
| chr5:132830617-132830747 | Rare:38 | ||||
| chr5:132866440-132866690 | Common:1; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133026534-133026754 | Common:4; Rare:49 | ||||
| chr5:133051849-133052216 | Rare:126 | ||||
| chr5:133052220-133052351 | Common:1; Rare:31 | ||||
| chr5:133968491-133968718 | Rare:98 | ||||
| chr5:134004510-134004900 | Common:2; Rare:133 | ||||
| chr5:134004904-134005030 | Rare:26 | ||||
| chr5:134225548-134225600 | Common:1; Rare:17 | ||||
| chr5:134226061-134226407 | Common:1; Rare:105 |