| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:131165164-131165382 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr5:131170651-131171013 | Common:1; Rare:87; Clinvar (benign):2 | ||||
| chr5:131635160-131635735 | Common:1; Rare:190 | ||||
| chr5:131796936-131797227 | Rare:83 | ||||
| chr5:132257487-132257708 | Common:7; Rare:52 | ||||
| chr5:132369604-132369964 | Common:7; Rare:117; Clinvar:6; Clinvar (benign):6 | ||||
| chr5:132410603-132410924 | Common:1; Rare:62 | ||||
| chr5:132556885-132557037 | Rare:60; Clinvar:1 | ||||
| chr5:132777215-132777432 | Rare:50 | ||||
| chr5:132866470-132866738 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132866758-132866981 | Common:1; Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:132963281-132963403 | Rare:25 | ||||
| chr5:132963489-132963844 | Common:1; Rare:89 | ||||
| chr5:133026519-133026799 | Common:5; Rare:65 | ||||
| chr5:133051589-133052366 | Common:4; Rare:245 |