| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11377273-11377416 | Rare:36; Clinvar (benign):3 | ||||
| chr19:11422264-11422478 | Common:1; Rare:57 | ||||
| chr19:11482122-11482332 | Rare:52 | ||||
| chr19:11482670-11482909 | Common:3; Rare:82 | ||||
| chr19:11568194-11568414 | Common:2; Rare:34 | ||||
| chr19:11568426-11568596 | Common:2; Rare:38 | ||||
| chr19:11583977-11584293 | Common:1; Rare:50 | ||||
| chr19:11639630-11639903 | Common:2; Rare:74 | ||||
| chr19:11694865-11695150 | Common:1; Rare:66 | ||||
| chr19:11737992-11738237 | Rare:50 | ||||
| chr19:11767802-11767983 | Rare:38 | ||||
| chr19:11987488-11987719 | Common:6; Rare:57 | ||||
| chr19:11987801-11987912 | Common:1; Rare:19 | ||||
| chr19:11988036-11988309 | Common:1; Rare:52 | ||||
| chr19:11988531-11988779 | Common:1; Rare:52 |