| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49362375-49362465 | Rare:20 | ||||
| chr19:49453024-49453311 | Common:2; Rare:88 | ||||
| chr19:49513102-49513403 | Common:1; Rare:69 | ||||
| chr19:49580528-49580688 | Rare:51 | ||||
| chr19:49641826-49642069 | Rare:70 | ||||
| chr19:49665716-49666018 | Common:3; Rare:137; Clinvar (pathogenic):1 | ||||
| chr19:49691019-49691140 | Rare:31 | ||||
| chr19:49808823-49808981 | Rare:53 | ||||
| chr19:49813233-49813467 | Common:1; Rare:68 | ||||
| chr19:49851068-49851120 | Rare:21 | ||||
| chr19:49854396-49854717 | Common:1; Rare:120 | ||||
| chr19:49867505-49867650 | Common:2; Rare:42; Clinvar:1 | ||||
| chr19:49877319-49877742 | Common:1; Rare:113 | ||||
| chr19:49877906-49878141 | Common:2; Rare:76 | ||||
| chr19:49929458-49929804 | Common:7; Rare:118 |