| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:49878943-49879263 | Common:3; Rare:104; Clinvar (benign):1 | ||||
| chr18:50281436-50281636 | Common:2; Rare:67 | ||||
| chr18:50878948-50879228 | Common:4; Rare:94 | ||||
| chr18:51028188-51028447 | Common:3; Rare:45 | ||||
| chr18:51030060-51030222 | Rare:53 | ||||
| chr18:54269676-54269821 | Common:1; Rare:25 | ||||
| chr18:62186938-62187320 | Common:5; Rare:106 | ||||
| chr18:63367112-63367318 | Common:1; Rare:74 | ||||
| chr18:63422371-63422548 | Rare:55 | ||||
| chr18:63587140-63587401 | Common:2; Rare:65 | ||||
| chr18:63969981-63970149 | Common:4; Rare:31 | ||||
| chr18:68715051-68715284 | Common:4; Rare:99 | ||||
| chr18:74291878-74292208 | Common:2; Rare:93 | ||||
| chr18:74496007-74496423 | Common:5; Rare:136 | ||||
| chr18:74597566-74597914 | Common:2; Rare:93 |