| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3451466-3451677 | Common:2; Rare:81 | ||||
| chr18:9102508-9102766 | Common:2; Rare:105; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136493-9136837 | Rare:133 | ||||
| chr18:11851212-11851473 | Common:2; Rare:102 | ||||
| chr18:11908276-11908411 | Rare:37 | ||||
| chr18:12702671-12703084 | Common:3; Rare:166 | ||||
| chr18:12884169-12884425 | Common:4; Rare:124 | ||||
| chr18:12947683-12948083 | Common:3; Rare:107 | ||||
| chr18:12991137-12991378 | Common:1; Rare:87 | ||||
| chr18:13726520-13726720 | Common:3; Rare:76 | ||||
| chr18:22933277-22933413 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr18:22933807-22933902 | Common:1; Rare:37 | ||||
| chr18:23453069-23453353 | Rare:98 | ||||
| chr18:23503287-23503547 | Common:2; Rare:94 | ||||
| chr18:24426493-24426763 | Common:5; Rare:110 |