| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49335130-49335487 | Common:1; Rare:66 | ||||
| chr19:49335560-49335759 | Common:2; Rare:63 | ||||
| chr19:49362347-49362477 | Rare:37 | ||||
| chr19:49447404-49447687 | Rare:88 | ||||
| chr19:49451599-49451851 | Common:1; Rare:61 | ||||
| chr19:49453094-49453318 | Common:1; Rare:70 | ||||
| chr19:49453450-49453612 | Rare:53 | ||||
| chr19:49513109-49513414 | Common:1; Rare:71 | ||||
| chr19:49527864-49528038 | Common:3; Rare:53 | ||||
| chr19:49560362-49560480 | Common:1; Rare:20 | ||||
| chr19:49580515-49580661 | Rare:53 | ||||
| chr19:49581234-49581424 | Common:1; Rare:38 | ||||
| chr19:49641834-49642054 | Rare:65 | ||||
| chr19:49665485-49666050 | Common:6; Rare:244; Clinvar (pathogenic):1 | ||||
| chr19:49690973-49691144 | Common:1; Rare:38 |