| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38974765-38974876 | Rare:18 | ||||
| chr19:39038336-39038433 | Rare:17 | ||||
| chr19:39046182-39046423 | Common:1; Rare:47 | ||||
| chr19:39320829-39321002 | Common:2; Rare:29 | ||||
| chr19:39402679-39402929 | Rare:67 | ||||
| chr19:39402991-39403038 | Rare:8 | ||||
| chr19:39403558-39403633 | Rare:14 | ||||
| chr19:39403685-39403899 | Rare:37 | ||||
| chr19:39403904-39404120 | Rare:53 | ||||
| chr19:39410162-39410199 | Rare:7 | ||||
| chr19:39440590-39440743 | Common:2; Rare:29 | ||||
| chr19:39444992-39445040 | Rare:13 | ||||
| chr19:39497784-39498133 | Common:5; Rare:87 | ||||
| chr19:39498327-39498378 | Rare:7 | ||||
| chr19:39507119-39507351 | Rare:104; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 |