| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:26549629-26550014 | Common:10; Rare:263 | ||||
| chr18:26656920-26657190 | Common:13; Rare:177 | ||||
| chr18:26657193-26657360 | Rare:97 | ||||
| chr18:27185260-27185470 | Common:3; Rare:76 | ||||
| chr18:28177699-28177806 | Rare:33 | ||||
| chr18:31101354-31101992 | Common:29; Rare:304; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr18:31102080-31102650 | Common:1; Rare:126; Clinvar:9 | ||||
| chr18:31498004-31498287 | Common:3; Rare:249; Clinvar:15; Clinvar (benign):18 | ||||
| chr18:31684630-31684890 | Rare:192 | ||||
| chr18:31685010-31685700 | Common:12; Rare:446 | ||||
| chr18:31942288-31942498 | Common:2; Rare:55 | ||||
| chr18:31943051-31943612 | Common:21; Rare:342 | ||||
| chr18:32018510-32018866 | Common:3; Rare:110 | ||||
| chr18:32091807-32092202 | Common:9; Rare:212 | ||||
| chr18:32092262-32092803 | Common:20; Rare:610 |