| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79395883-79396021 | Rare:36 | ||||
| chr18:79400162-79400393 | Common:11; Rare:253 | ||||
| chr18:79678969-79679630 | Common:14; Rare:634 | ||||
| chr18:79679559-79679901 | Common:6; Rare:203 | ||||
| chr18:79951592-79951906 | Common:10; Rare:319 | ||||
| chr18:79964467-79964713 | Common:3; Rare:143 | ||||
| chr18:79988406-79988912 | Common:12; Rare:328; Clinvar (pathogenic):6 | ||||
| chr18:80033582-80034778 | Common:42; Rare:997 | ||||
| chr18:80108755-80109084 | Common:1; Rare:80 | ||||
| chr18:80109163-80109430 | Rare:89 | ||||
| chr18:80109604-80110170 | Common:2; Rare:199 | ||||
| chr18:80247452-80247751 | Common:2; Rare:82 | ||||
| chr19:290519-290773 | Common:2; Rare:76 | ||||
| chr19:291094-291494 | Common:3; Rare:226 | ||||
| chr19:344716-345016 | Common:11; Rare:230 |