| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3448444-3448471 | Rare:5 | ||||
| chr18:3449417-3449798 | Common:5; Rare:96 | ||||
| chr18:3450059-3450397 | Common:1; Rare:94 | ||||
| chr18:9102494-9102772 | Common:2; Rare:112; Clinvar:6; Clinvar (benign):2 | ||||
| chr18:9136522-9136915 | Rare:148 | ||||
| chr18:9137051-9137342 | Common:3; Rare:118 | ||||
| chr18:9474791-9475174 | Common:4; Rare:98 | ||||
| chr18:9475289-9475712 | Common:5; Rare:111 | ||||
| chr18:9708042-9708339 | Common:5; Rare:74 | ||||
| chr18:9914191-9914332 | Rare:60 | ||||
| chr18:11851246-11851808 | Common:3; Rare:198 | ||||
| chr18:11851893-11851924 | Rare:10 | ||||
| chr18:11908274-11908442 | Rare:50 | ||||
| chr18:11980869-11981031 | Common:3; Rare:54 | ||||
| chr18:12027708-12028150 | Common:5; Rare:91 |