| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:612191-612357 | Rare:67 | ||||
| chr5:1494829-1495082 | Rare:86 | ||||
| chr5:1495316-1495426 | Common:2; Rare:42 | ||||
| chr5:1799778-1799961 | Common:8; Rare:90 | ||||
| chr5:1801300-1801535 | Common:4; Rare:124; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:5422337-5422702 | Common:2; Rare:120 | ||||
| chr5:6378466-6378678 | Rare:87 | ||||
| chr5:6632981-6633460 | Common:8; Rare:155; Clinvar:10; Clinvar (benign):4 | ||||
| chr5:7868995-7869227 | Common:2; Rare:122; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:10249879-10249937 | Common:13; Rare:71 | ||||
| chr5:10250154-10250399 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353594-10353910 | Common:3; Rare:116 | ||||
| chr5:16616967-16617182 | Common:2; Rare:58; Clinvar (benign):5 | ||||
| chr5:31532000-31532332 | Common:3; Rare:84 | ||||
| chr5:32174252-32174421 | Common:1; Rare:63 |