| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:8705607-8706129 | Common:3; Rare:145 | ||||
| chr18:9102248-9102781 | Common:13; Rare:951; Clinvar:42; Clinvar (benign):14 | ||||
| chr18:9103130-9103943 | Common:10; Rare:399 | ||||
| chr18:9104066-9104466 | Common:3; Rare:93 | ||||
| chr18:9135915-9136898 | Common:14; Rare:1314 | ||||
| chr18:9136890-9137640 | Common:26; Rare:959 | ||||
| chr18:9137804-9138002 | Common:3; Rare:52 | ||||
| chr18:9334259-9335183 | Common:10; Rare:666 | ||||
| chr18:9335120-9336111 | Common:4; Rare:261 | ||||
| chr18:9474462-9474862 | Common:4; Rare:81 | ||||
| chr18:9474849-9475029 | Common:2; Rare:80 | ||||
| chr18:9475124-9475670 | Common:47; Rare:851 | ||||
| chr18:9475720-9476110 | Common:12; Rare:271 | ||||
| chr18:9476358-9476758 | Common:2; Rare:75 | ||||
| chr18:9613510-9614250 | Common:6; Rare:272 |