| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:32114146-32114269 | Common:1; Rare:18 | ||||
| chr18:32469389-32469555 | Rare:35 | ||||
| chr18:37242893-37243151 | Common:1; Rare:39 | ||||
| chr18:39313960-39314252 | Common:1; Rare:53 | ||||
| chr18:44682332-44682543 | Common:1; Rare:36 | ||||
| chr18:44964793-44964925 | Common:1; Rare:29 | ||||
| chr18:45686729-45687062 | Common:3; Rare:60 | ||||
| chr18:46087456-46087809 | Common:3; Rare:90; Clinvar (benign):2 | ||||
| chr18:54899739-54899932 | Common:1; Rare:33 | ||||
| chr18:55319513-55319747 | Rare:40 | ||||
| chr18:56573115-56573130 | Rare:7 | ||||
| chr18:57630215-57630368 | Common:1; Rare:43 | ||||
| chr18:57652689-57652777 | Common:1; Rare:20; Clinvar (benign):2 | ||||
| chr18:57658212-57658484 | Common:2; Rare:36 | ||||
| chr18:57658817-57658992 | Common:1; Rare:24 |