| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:80487899-80488023 | Rare:34 | ||||
| chr5:80488042-80488132 | Rare:35 | ||||
| chr5:80654539-80654714 | Common:5; Rare:102 | ||||
| chr5:81233009-81233339 | Common:1; Rare:68 | ||||
| chr5:81301470-81301668 | Common:5; Rare:68 | ||||
| chr5:81971752-81972081 | Common:3; Rare:126 | ||||
| chr5:82278319-82278687 | Common:3; Rare:119 | ||||
| chr5:83077334-83077619 | Common:1; Rare:85 | ||||
| chr5:83471296-83471834 | Common:4; Rare:129; Clinvar:2 | ||||
| chr5:84384361-84384719 | Rare:133 | ||||
| chr5:84385116-84385384 | Common:2; Rare:44 | ||||
| chr5:86617749-86618113 | Common:2; Rare:114 | ||||
| chr5:87267679-87267995 | Common:4; Rare:119 | ||||
| chr5:87268598-87268910 | Common:1; Rare:144; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr5:87412643-87413133 | Common:6; Rare:168 |