| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:26090510-26090980 | Common:5; Rare:181 | ||||
| chr18:26091128-26091281 | Common:2; Rare:41 | ||||
| chr18:28176973-28177295 | Common:3; Rare:156 | ||||
| chr18:31101901-31102031 | Common:1; Rare:35; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr18:31102264-31102472 | Common:1; Rare:56; Clinvar:6 | ||||
| chr18:31318120-31318243 | Common:1; Rare:19 | ||||
| chr18:34976770-34977067 | Common:2; Rare:60 | ||||
| chr18:35041175-35041452 | Common:2; Rare:91 | ||||
| chr18:35240912-35241055 | Common:2; Rare:48 | ||||
| chr18:35290188-35290377 | Common:2; Rare:68 | ||||
| chr18:35344388-35344579 | Common:2; Rare:62 | ||||
| chr18:35497900-35498006 | Common:1; Rare:36 | ||||
| chr18:35972472-35972736 | Common:3; Rare:90 | ||||
| chr18:36129117-36129471 | Common:4; Rare:101 | ||||
| chr18:36129817-36129934 | Rare:49 |