| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13218651-13218790 | Common:1; Rare:31 | ||||
| chr18:13612613-13612622 | Rare:1 | ||||
| chr18:13726370-13726724 | Common:4; Rare:125 | ||||
| chr18:21111140-21111353 | Common:1; Rare:51 | ||||
| chr18:21111514-21111977 | Common:2; Rare:140 | ||||
| chr18:21242172-21242406 | Common:1; Rare:94 | ||||
| chr18:21600185-21600251 | Common:1; Rare:17 | ||||
| chr18:21600422-21600521 | Rare:25 | ||||
| chr18:21600625-21600928 | Common:2; Rare:80 | ||||
| chr18:21704674-21704991 | Common:3; Rare:100 | ||||
| chr18:21740569-21740853 | Common:2; Rare:88 | ||||
| chr18:22169452-22169608 | Rare:42 | ||||
| chr18:22914025-22914169 | Rare:28 | ||||
| chr18:22933277-22933426 | Common:2; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933748-22933902 | Common:1; Rare:65 |