| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:31498062-31498279 | Common:1; Rare:77; Clinvar:5; Clinvar (benign):6 | ||||
| chr18:31943078-31943380 | Common:7; Rare:97 | ||||
| chr18:32092384-32092727 | Common:5; Rare:156 | ||||
| chr18:35041332-35041501 | Rare:72 | ||||
| chr18:35240912-35241094 | Common:2; Rare:69 | ||||
| chr18:35290178-35290391 | Common:2; Rare:76 | ||||
| chr18:35344394-35344505 | Common:2; Rare:38 | ||||
| chr18:35377266-35377406 | Common:4; Rare:39 | ||||
| chr18:35972472-35972722 | Common:3; Rare:80 | ||||
| chr18:36129266-36129531 | Common:3; Rare:83 | ||||
| chr18:36129827-36129982 | Rare:69 | ||||
| chr18:36187408-36187562 | Common:4; Rare:57 | ||||
| chr18:36828736-36829283 | Common:3; Rare:216 | ||||
| chr18:44680700-44680995 | Common:1; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:45967243-45967465 | Rare:83 |