| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:55534627-55534840 | Common:3; Rare:68 | ||||
| chr5:55534948-55535189 | Common:1; Rare:82 | ||||
| chr5:55994797-55995199 | Rare:139 | ||||
| chr5:56815254-56815576 | Common:3; Rare:118 | ||||
| chr5:56909400-56909656 | Common:4; Rare:73 | ||||
| chr5:56909824-56910077 | Common:2; Rare:62 | ||||
| chr5:56952095-56952315 | Rare:80 | ||||
| chr5:57173440-57174199 | Common:3; Rare:268 | ||||
| chr5:58460038-58460242 | Common:5; Rare:84 | ||||
| chr5:59039074-59039199 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr5:59039742-59039912 | Common:3; Rare:50 | ||||
| chr5:59275970-59276224 | Common:4; Rare:40 | ||||
| chr5:59768487-59768723 | Rare:62 | ||||
| chr5:60488050-60488343 | Rare:55 | ||||
| chr5:60700089-60700249 | Common:1; Rare:61 |