| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34404288-34404427 | Common:2; Rare:50 | ||||
| chr19:34428312-34428507 | Rare:77 | ||||
| chr19:34677538-34677762 | Common:5; Rare:67 | ||||
| chr19:34733834-34734280 | Common:3; Rare:123 | ||||
| chr19:34734483-34734579 | Rare:21 | ||||
| chr19:34926831-34926996 | Common:1; Rare:57 | ||||
| chr19:35155155-35155230 | Rare:15 | ||||
| chr19:35266946-35267279 | Common:1; Rare:121 | ||||
| chr19:35319067-35319412 | Common:3; Rare:56 | ||||
| chr19:35545446-35545726 | Common:4; Rare:91 | ||||
| chr19:35628809-35629103 | Common:4; Rare:89 | ||||
| chr19:35648110-35648412 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35745393-35745703 | Rare:89 | ||||
| chr19:35748276-35748625 | Common:3; Rare:101 | ||||
| chr19:35757874-35758201 | Common:2; Rare:97 |