| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1374361-1374481 | Common:2; Rare:36 | ||||
| chr19:1400450-1400834 | Common:10; Rare:164 | ||||
| chr19:1418028-1418601 | Common:4; Rare:204 | ||||
| chr19:1876129-1876267 | Common:1; Rare:108 | ||||
| chr19:2046150-2046434 | Common:4; Rare:192 | ||||
| chr19:2059506-2060470 | Common:9; Rare:379 | ||||
| chr19:2061432-2061754 | Common:4; Rare:208 | ||||
| chr19:2115180-2115560 | Common:4; Rare:140 | ||||
| chr19:2165098-2165822 | Common:6; Rare:349 | ||||
| chr19:2167430-2167715 | Common:2; Rare:125 | ||||
| chr19:2168771-2169276 | Common:26; Rare:372 | ||||
| chr19:2171777-2172177 | Common:4; Rare:184 | ||||
| chr19:2253152-2253338 | Common:6; Rare:79 | ||||
| chr19:2438220-2438710 | Common:2; Rare:174; Clinvar:10; Clinvar (benign):1 | ||||
| chr19:2540674-2541150 | Common:8; Rare:204 |