| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:80256041-80256260 | Common:1; Rare:88 | ||||
| chr5:80407864-80408101 | Common:1; Rare:87 | ||||
| chr5:80487963-80488118 | Common:1; Rare:55 | ||||
| chr5:80654562-80654700 | Common:5; Rare:86 | ||||
| chr5:81301513-81301664 | Common:4; Rare:52 | ||||
| chr5:81971752-81972059 | Common:3; Rare:118 | ||||
| chr5:81972215-81972295 | Common:1; Rare:20 | ||||
| chr5:82278319-82278692 | Common:4; Rare:121 | ||||
| chr5:83077339-83077615 | Common:1; Rare:79 | ||||
| chr5:84384378-84384696 | Rare:115 | ||||
| chr5:87268673-87268964 | Common:1; Rare:132; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr5:88883170-88883351 | Rare:65; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:90409690-90410024 | Common:6; Rare:112 | ||||
| chr5:90474739-90474931 | Common:1; Rare:77 | ||||
| chr5:90529551-90529877 | Common:2; Rare:118 |