| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:2571478-2571616 | Rare:38 | ||||
| chr18:2655532-2655726 | Common:4; Rare:97 | ||||
| chr18:3013107-3013407 | Common:3; Rare:114 | ||||
| chr18:3247281-3247507 | Common:3; Rare:67 | ||||
| chr18:3247758-3247907 | Rare:53 | ||||
| chr18:3261815-3262223 | Common:6; Rare:131 | ||||
| chr18:3449365-3449604 | Common:2; Rare:61 | ||||
| chr18:3449960-3450196 | Rare:70 | ||||
| chr18:8707644-8707866 | Rare:42 | ||||
| chr18:9102441-9102765 | Common:2; Rare:134; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136509-9136855 | Rare:132 | ||||
| chr18:9913785-9914039 | Common:1; Rare:92 | ||||
| chr18:9914200-9914256 | Rare:31 | ||||
| chr18:11851099-11851440 | Common:2; Rare:110 | ||||
| chr18:11908267-11908392 | Rare:34 |