| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45584201-45584646 | Common:3; Rare:128; Clinvar:1 | ||||
| chr19:45584741-45585087 | Common:4; Rare:129; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45639357-45639488 | Common:1; Rare:37 | ||||
| chr19:45642127-45642376 | Rare:79 | ||||
| chr19:45642386-45642660 | Common:2; Rare:67 | ||||
| chr19:45668055-45668289 | Common:2; Rare:43 | ||||
| chr19:45691849-45692029 | Rare:72 | ||||
| chr19:45692484-45692772 | Common:3; Rare:81 | ||||
| chr19:45730788-45731186 | Common:1; Rare:85 | ||||
| chr19:45769198-45769689 | Common:2; Rare:202 | ||||
| chr19:45792081-45792379 | Rare:73 | ||||
| chr19:45792723-45792814 | Rare:43 | ||||
| chr19:45862565-45862692 | Rare:35 | ||||
| chr19:45863073-45863460 | Common:4; Rare:114 | ||||
| chr19:45864115-45864337 | Common:2; Rare:50 |