| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:59359183-59359519 | Common:4; Rare:155; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:62186938-62187334 | Common:5; Rare:108 | ||||
| chr18:62522850-62523085 | Common:4; Rare:80 | ||||
| chr18:62523958-62524093 | Rare:42 | ||||
| chr18:62526717-62526929 | Common:2; Rare:99 | ||||
| chr18:62715144-62715498 | Common:3; Rare:98 | ||||
| chr18:63367081-63367348 | Common:1; Rare:96 | ||||
| chr18:63422336-63422665 | Common:1; Rare:89 | ||||
| chr18:63490534-63490600 | Rare:16 | ||||
| chr18:68714982-68715296 | Common:7; Rare:134 | ||||
| chr18:68823287-68823409 | Common:2; Rare:21 | ||||
| chr18:69643546-69643693 | Common:1; Rare:15 | ||||
| chr18:70205648-70205750 | Common:2; Rare:48; Clinvar (benign):2 | ||||
| chr18:70206000-70206223 | Rare:72 | ||||
| chr18:70288751-70289066 | Common:4; Rare:98 |