| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:49813819-49814200 | Common:1; Rare:156 | ||||
| chr18:50274987-50275231 | Rare:86 | ||||
| chr18:50281423-50281559 | Rare:52 | ||||
| chr18:50287821-50288077 | Common:4; Rare:51 | ||||
| chr18:50878872-50879239 | Common:4; Rare:123 | ||||
| chr18:51030052-51030227 | Rare:57 | ||||
| chr18:54269494-54269624 | Common:1; Rare:70 | ||||
| chr18:54828346-54828560 | Rare:52 | ||||
| chr18:54828566-54828618 | Rare:8 | ||||
| chr18:55589774-55589908 | Rare:41 | ||||
| chr18:56651133-56651410 | Common:4; Rare:73 | ||||
| chr18:57621724-57621976 | Common:3; Rare:89 | ||||
| chr18:57803031-57803253 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:58044963-58045179 | Common:2; Rare:62 | ||||
| chr18:58045562-58045745 | Rare:50 |