| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31318018-31318348 | Common:2; Rare:69; Clinvar (benign):1 | ||||
| chr18:31343271-31343595 | Rare:80 | ||||
| chr18:31498050-31498259 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):5 | ||||
| chr18:31943098-31943375 | Common:7; Rare:89 | ||||
| chr18:32092390-32092696 | Common:4; Rare:135 | ||||
| chr18:35290205-35290391 | Common:1; Rare:68 | ||||
| chr18:36129212-36129471 | Common:4; Rare:79 | ||||
| chr18:36129788-36129928 | Common:1; Rare:54 | ||||
| chr18:36187451-36187525 | Common:2; Rare:33 | ||||
| chr18:36828748-36829177 | Common:3; Rare:171 | ||||
| chr18:45967261-45967483 | Rare:79 | ||||
| chr18:46104135-46104399 | Common:3; Rare:75; Clinvar (benign):1 | ||||
| chr18:47150456-47150546 | Common:2; Rare:33 | ||||
| chr18:49487132-49487322 | Common:3; Rare:74 | ||||
| chr18:49813826-49814273 | Common:1; Rare:184 |