| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48993553-48993913 | Common:5; Rare:94 | ||||
| chr19:49085097-49085531 | Common:3; Rare:170 | ||||
| chr19:49361515-49361792 | Rare:50 | ||||
| chr19:49362367-49362483 | Rare:31 | ||||
| chr19:49453094-49453311 | Common:1; Rare:69 | ||||
| chr19:49453473-49453612 | Rare:39 | ||||
| chr19:49487280-49487644 | Common:5; Rare:130 | ||||
| chr19:49527817-49528031 | Common:3; Rare:72 | ||||
| chr19:49580528-49580670 | Rare:48 | ||||
| chr19:49641826-49642077 | Rare:70 | ||||
| chr19:49665725-49666034 | Common:3; Rare:143; Clinvar (pathogenic):1 | ||||
| chr19:49690980-49691150 | Common:2; Rare:39 | ||||
| chr19:49851068-49851154 | Rare:34 | ||||
| chr19:49877293-49877724 | Common:1; Rare:112 | ||||
| chr19:49877903-49878179 | Common:2; Rare:91 |