| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13484000-13484049 | Rare:9 | ||||
| chr18:22168419-22168679 | Rare:54 | ||||
| chr18:23526471-23526737 | Rare:65 | ||||
| chr18:32093364-32093503 | Common:1; Rare:39 | ||||
| chr18:32770550-32770760 | Common:1; Rare:52 | ||||
| chr18:45686751-45687066 | Common:3; Rare:55 | ||||
| chr18:46019323-46019563 | Common:3; Rare:43 | ||||
| chr18:46087204-46087441 | Rare:55; Clinvar (pathogenic):1 | ||||
| chr18:46089565-46089879 | Common:2; Rare:83; Clinvar (benign):2 | ||||
| chr18:46089906-46090208 | Common:4; Rare:79; Clinvar (benign):2 | ||||
| chr18:46868470-46868644 | Rare:37 | ||||
| chr18:55892711-55893059 | Common:4; Rare:99 | ||||
| chr18:57630023-57630401 | Common:5; Rare:85 | ||||
| chr18:57659526-57659600 | Common:3; Rare:12 | ||||
| chr18:57662592-57662833 | Common:1; Rare:43; Clinvar (pathogenic):1 |