| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21111487-21111971 | Common:2; Rare:137 | ||||
| chr18:21242195-21242376 | Common:1; Rare:73 | ||||
| chr18:21600632-21600838 | Rare:51 | ||||
| chr18:22169321-22169614 | Common:2; Rare:78 | ||||
| chr18:22933141-22933395 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:22933781-22933889 | Common:1; Rare:43 | ||||
| chr18:23453085-23453341 | Rare:90 | ||||
| chr18:23503298-23503619 | Common:4; Rare:135 | ||||
| chr18:23586387-23586550 | Common:2; Rare:76; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:25352045-25352406 | Common:2; Rare:144 | ||||
| chr18:28176995-28177295 | Common:3; Rare:143 | ||||
| chr18:32092333-32092727 | Common:6; Rare:179 | ||||
| chr18:34493286-34493452 | Rare:29 | ||||
| chr18:34593188-34593437 | Rare:49 | ||||
| chr18:35290188-35290384 | Common:2; Rare:69 |