| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:123511891-123512562 | Common:3; Rare:209 | ||||
| chr5:124746267-124746582 | Common:2; Rare:53 | ||||
| chr5:124746589-124746687 | Rare:24 | ||||
| chr5:124746740-124746860 | Common:1; Rare:23 | ||||
| chr5:126423347-126423619 | Rare:78 | ||||
| chr5:126595123-126595475 | Common:5; Rare:125; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):3 | ||||
| chr5:127030498-127030710 | Common:2; Rare:52 | ||||
| chr5:127517566-127517952 | Common:4; Rare:121 | ||||
| chr5:128082956-128083481 | Common:8; Rare:167 | ||||
| chr5:128538166-128538354 | Common:5; Rare:67 | ||||
| chr5:131162668-131162723 | Rare:15; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:131165095-131165376 | Common:2; Rare:103; Clinvar (benign):2 | ||||
| chr5:131170715-131171011 | Common:1; Rare:60; Clinvar (benign):2 | ||||
| chr5:131635138-131635424 | Common:1; Rare:109 | ||||
| chr5:131796902-131797195 | Rare:87 |