| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49639967-49640593 | Common:1; Rare:185; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:49641820-49642126 | Rare:87 | ||||
| chr19:49665327-49665418 | Rare:23 | ||||
| chr19:49665428-49666043 | Common:6; Rare:265; Clinvar (pathogenic):1 | ||||
| chr19:49677167-49677319 | Common:1; Rare:60 | ||||
| chr19:49851068-49851211 | Common:1; Rare:57 | ||||
| chr19:49854371-49854696 | Common:2; Rare:121 | ||||
| chr19:49856692-49857127 | Common:3; Rare:181; Clinvar (benign):1 | ||||
| chr19:49859986-49860449 | Common:3; Rare:195 | ||||
| chr19:49866994-49867087 | Rare:33; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:49867189-49867405 | Common:2; Rare:72; Clinvar:1; Clinvar (benign):5 | ||||
| chr19:49867539-49867687 | Common:3; Rare:41 | ||||
| chr19:49876225-49876267 | Rare:14 | ||||
| chr19:49877220-49877724 | Common:2; Rare:126 | ||||
| chr19:49877913-49878145 | Common:2; Rare:74 |