| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:77087196-77087359 | Rare:34 | ||||
| chr5:78360390-78360636 | Common:5; Rare:94 | ||||
| chr5:79069575-79069657 | Rare:22; Clinvar (benign):2 | ||||
| chr5:79236008-79236173 | Common:1; Rare:64 | ||||
| chr5:79991247-79991298 | Rare:16 | ||||
| chr5:80487938-80488129 | Common:1; Rare:64 | ||||
| chr5:81301518-81301675 | Common:4; Rare:55 | ||||
| chr5:82278319-82278670 | Common:3; Rare:111 | ||||
| chr5:83077336-83077618 | Common:1; Rare:82 | ||||
| chr5:84384235-84384466 | Rare:69 | ||||
| chr5:84384503-84384690 | Rare:75 | ||||
| chr5:84384712-84384927 | Rare:74 | ||||
| chr5:90529515-90529811 | Common:1; Rare:110 | ||||
| chr5:94111510-94111684 | Common:1; Rare:58 | ||||
| chr5:95554946-95555199 | Rare:69 |