| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19033475-19033653 | Common:2; Rare:55 | ||||
| chr19:19033796-19033928 | Common:1; Rare:36 | ||||
| chr19:19095838-19096058 | Common:2; Rare:57 | ||||
| chr19:19192096-19192268 | Common:1; Rare:56 | ||||
| chr19:19192632-19193008 | Common:3; Rare:87; Clinvar (benign):1 | ||||
| chr19:19203357-19203539 | Rare:53 | ||||
| chr19:19320480-19320851 | Common:4; Rare:133 | ||||
| chr19:19516157-19516331 | Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19668606-19668856 | Common:1; Rare:67 | ||||
| chr19:19821668-19821878 | Common:1; Rare:72 | ||||
| chr19:21141853-21142094 | Rare:66 | ||||
| chr19:22634115-22634358 | Common:7; Rare:71 | ||||
| chr19:29213089-29213292 | Common:5; Rare:65 | ||||
| chr19:29606186-29606323 | Rare:46 | ||||
| chr19:29665252-29665496 | Common:4; Rare:87 |