| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49335289-49335406 | Rare:18 | ||||
| chr19:49362367-49362520 | Rare:42 | ||||
| chr19:49453094-49453305 | Common:1; Rare:67 | ||||
| chr19:49580528-49580656 | Rare:43 | ||||
| chr19:49641826-49642031 | Rare:57 | ||||
| chr19:49665752-49666004 | Common:3; Rare:118; Clinvar (pathogenic):1 | ||||
| chr19:49867518-49867633 | Common:2; Rare:39; Clinvar:1 | ||||
| chr19:49877246-49877724 | Common:2; Rare:119 | ||||
| chr19:50476267-50476556 | Rare:134 | ||||
| chr19:50723214-50723377 | Common:2; Rare:41 | ||||
| chr19:51001158-51001212 | Common:1; Rare:12 | ||||
| chr19:51019675-51019957 | Common:5; Rare:51 | ||||
| chr19:51026574-51026756 | Common:2; Rare:48 | ||||
| chr19:51027477-51027707 | Common:1; Rare:48 | ||||
| chr19:51034891-51035237 | Common:3; Rare:70 |