| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42302301-42302410 | Rare:39 | ||||
| chr19:42302416-42302509 | Rare:21 | ||||
| chr19:42302513-42302679 | Rare:49 | ||||
| chr19:42302768-42302857 | Common:3; Rare:14 | ||||
| chr19:42325405-42325675 | Rare:67 | ||||
| chr19:42423092-42423381 | Common:2; Rare:69 | ||||
| chr19:42423526-42423753 | Common:4; Rare:81 | ||||
| chr19:42424184-42424402 | Common:1; Rare:74 | ||||
| chr19:42427337-42427444 | Rare:21 | ||||
| chr19:42528431-42528542 | Common:2; Rare:32 | ||||
| chr19:42739460-42739566 | Rare:48 | ||||
| chr19:43414662-43414955 | Common:2; Rare:80 | ||||
| chr19:43504587-43504701 | Common:1; Rare:21 | ||||
| chr19:43527210-43527303 | Common:4; Rare:33; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:43575417-43575760 | Common:2; Rare:105 |