| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:79069652-79069775 | Rare:44 | ||||
| chr5:79235953-79236134 | Common:2; Rare:74 | ||||
| chr5:79514554-79514676 | Rare:31 | ||||
| chr5:79612370-79612655 | Rare:89 | ||||
| chr5:79991215-79991359 | Rare:46 | ||||
| chr5:80256039-80256231 | Common:1; Rare:78 | ||||
| chr5:80407890-80408096 | Common:1; Rare:77 | ||||
| chr5:80487878-80488124 | Common:1; Rare:76 | ||||
| chr5:80654559-80654738 | Common:5; Rare:113 | ||||
| chr5:80654916-80655158 | Common:4; Rare:91; Clinvar (benign):2 | ||||
| chr5:81301479-81301693 | Common:5; Rare:74 | ||||
| chr5:81971787-81972059 | Common:3; Rare:108 | ||||
| chr5:82278319-82278705 | Common:4; Rare:127 | ||||
| chr5:83077330-83077633 | Common:1; Rare:91 | ||||
| chr5:84384373-84384722 | Rare:129 |