| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:11689857-11689969 | Rare:36; Clinvar (benign):1 | ||||
| chr18:11690100-11690182 | Common:1; Rare:17 | ||||
| chr18:11851227-11851484 | Common:3; Rare:98 | ||||
| chr18:11857287-11857851 | Common:1; Rare:113 | ||||
| chr18:11908234-11908569 | Common:2; Rare:91 | ||||
| chr18:11908615-11908909 | Common:3; Rare:76 | ||||
| chr18:11909663-11909743 | Common:1; Rare:10 | ||||
| chr18:11980495-11980743 | Common:6; Rare:60 | ||||
| chr18:11980750-11981046 | Common:4; Rare:92 | ||||
| chr18:11981054-11981785 | Common:5; Rare:212 | ||||
| chr18:12308041-12308356 | Common:4; Rare:122 | ||||
| chr18:12308440-12308660 | Common:4; Rare:59 | ||||
| chr18:12308676-12308833 | Common:2; Rare:60 | ||||
| chr18:12376704-12377027 | Rare:104; Clinvar (benign):2 | ||||
| chr18:12377052-12378000 | Common:9; Rare:251; Clinvar:1; Clinvar (benign):8 |