| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:79991036-79991356 | Rare:115 | ||||
| chr5:80256028-80256267 | Common:1; Rare:96 | ||||
| chr5:80407872-80408100 | Common:1; Rare:82 | ||||
| chr5:80487910-80488126 | Common:1; Rare:69 | ||||
| chr5:80654501-80654714 | Common:5; Rare:120 | ||||
| chr5:81301474-81301675 | Common:5; Rare:68 | ||||
| chr5:81751089-81751415 | Common:1; Rare:95 | ||||
| chr5:81971972-81972322 | Common:2; Rare:119 | ||||
| chr5:82278319-82278702 | Common:4; Rare:126 | ||||
| chr5:83077330-83077631 | Common:1; Rare:91 | ||||
| chr5:84384378-84384728 | Rare:128 | ||||
| chr5:86617816-86618118 | Common:2; Rare:105 | ||||
| chr5:87267719-87267995 | Common:4; Rare:95 | ||||
| chr5:87268821-87269019 | Rare:72; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:87412798-87412966 | Common:3; Rare:57 |