| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22170677-22170737 | Rare:12 | ||||
| chr18:22170759-22170914 | Common:1; Rare:24 | ||||
| chr18:22933141-22933466 | Common:4; Rare:107; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933807-22933894 | Common:1; Rare:33 | ||||
| chr18:23453069-23453345 | Rare:95 | ||||
| chr18:23503300-23503603 | Common:4; Rare:123 | ||||
| chr18:23586387-23586531 | Common:2; Rare:65; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24271212-24271347 | Common:2; Rare:21 | ||||
| chr18:24271632-24272022 | Common:2; Rare:99 | ||||
| chr18:24397784-24397984 | Common:2; Rare:83 | ||||
| chr18:24426620-24426775 | Common:3; Rare:62 | ||||
| chr18:25350995-25351152 | Rare:57 | ||||
| chr18:25352050-25352410 | Common:2; Rare:143 | ||||
| chr18:28159169-28159300 | Rare:23 | ||||
| chr18:28176968-28177295 | Common:3; Rare:158 |