| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3451459-3451687 | Common:2; Rare:84 | ||||
| chr18:5196788-5196903 | Common:1; Rare:23 | ||||
| chr18:5197568-5197675 | Common:1; Rare:20 | ||||
| chr18:5197680-5197900 | Common:5; Rare:37 | ||||
| chr18:5296929-5297010 | Rare:28 | ||||
| chr18:9102519-9102764 | Common:1; Rare:100; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136225-9136353 | Common:2; Rare:35 | ||||
| chr18:9136603-9137042 | Rare:162 | ||||
| chr18:9474849-9475027 | Common:1; Rare:44 | ||||
| chr18:9475442-9475670 | Common:2; Rare:58 | ||||
| chr18:9615030-9615112 | Rare:25 | ||||
| chr18:9615192-9615436 | Common:1; Rare:38 | ||||
| chr18:9913832-9914053 | Common:1; Rare:81 | ||||
| chr18:9914198-9914280 | Rare:43 | ||||
| chr18:10455110-10455192 | Common:1; Rare:23 |