| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:6729947-6730038 | Common:1; Rare:29 | ||||
| chr18:7117745-7117933 | Common:4; Rare:61 | ||||
| chr18:9102483-9102796 | Common:2; Rare:128; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136603-9136882 | Rare:110 | ||||
| chr18:9334419-9334894 | Common:1; Rare:118 | ||||
| chr18:9474831-9474978 | Common:1; Rare:33 | ||||
| chr18:9475209-9475720 | Common:8; Rare:132 | ||||
| chr18:9615030-9615167 | Common:1; Rare:36 | ||||
| chr18:9914201-9914280 | Rare:43 | ||||
| chr18:10455081-10455192 | Common:2; Rare:35 | ||||
| chr18:10526372-10526418 | Common:1; Rare:21 | ||||
| chr18:11851277-11851446 | Rare:55 | ||||
| chr18:11857254-11857501 | Rare:47 | ||||
| chr18:11908262-11908437 | Rare:51 | ||||
| chr18:11980855-11981031 | Common:4; Rare:57 |