| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19033482-19033646 | Common:2; Rare:51 | ||||
| chr19:19033819-19033920 | Common:1; Rare:30 | ||||
| chr19:19192118-19192268 | Common:1; Rare:49 | ||||
| chr19:19192587-19192925 | Common:2; Rare:89 | ||||
| chr19:19320520-19320850 | Common:4; Rare:113 | ||||
| chr19:19385911-19386041 | Rare:55 | ||||
| chr19:19516147-19516287 | Rare:93; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:29213138-29213205 | Common:1; Rare:25 | ||||
| chr19:32675144-32675410 | Common:3; Rare:87 | ||||
| chr19:32971893-32972272 | Common:4; Rare:109 | ||||
| chr19:33373553-33373845 | Common:2; Rare:93 | ||||
| chr19:33521749-33521948 | Rare:65; Clinvar:5 | ||||
| chr19:34254511-34254601 | Rare:25 | ||||
| chr19:34677538-34677742 | Common:5; Rare:61 | ||||
| chr19:34734044-34734260 | Common:2; Rare:65 |