| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:79951585-79951913 | Common:4; Rare:132 | ||||
| chr18:79964508-79964685 | Common:1; Rare:53 | ||||
| chr18:79988088-79988249 | Rare:62 | ||||
| chr18:79988297-79988750 | Common:5; Rare:153; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr18:80033388-80033569 | Common:1; Rare:43 | ||||
| chr18:80033864-80033993 | Common:3; Rare:24 | ||||
| chr18:80034165-80034507 | Common:5; Rare:127 | ||||
| chr18:80034604-80034781 | Rare:64 | ||||
| chr18:80108771-80109123 | Common:2; Rare:84 | ||||
| chr18:80109157-80109417 | Rare:86 | ||||
| chr18:80109623-80109804 | Rare:50 | ||||
| chr18:80246978-80247023 | Rare:12 | ||||
| chr18:80247055-80247088 | Rare:7 | ||||
| chr18:80247475-80247739 | Common:1; Rare:76 | ||||
| chr19:291334-291657 | Common:7; Rare:52 |