| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:9708004-9708355 | Common:5; Rare:86 | ||||
| chr18:9914198-9914329 | Rare:58 | ||||
| chr18:11851090-11851490 | Common:4; Rare:133 | ||||
| chr18:11908254-11908383 | Rare:37 | ||||
| chr18:12307937-12308339 | Common:6; Rare:149 | ||||
| chr18:12702658-12703098 | Common:3; Rare:177 | ||||
| chr18:12947688-12948098 | Common:3; Rare:116 | ||||
| chr18:12991078-12991397 | Common:2; Rare:119 | ||||
| chr18:13726462-13726726 | Common:3; Rare:102 | ||||
| chr18:21600655-21600852 | Rare:46 | ||||
| chr18:22933759-22933867 | Common:1; Rare:46 | ||||
| chr18:23453156-23453376 | Rare:77 | ||||
| chr18:23503293-23503576 | Common:2; Rare:106 | ||||
| chr18:23586383-23586537 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24426620-24426765 | Common:3; Rare:61 |