| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41218670-41219098 | Common:9; Rare:93 | ||||
| chr19:41219183-41219207 | |||||
| chr19:41219212-41219566 | Common:2; Rare:104 | ||||
| chr19:41219749-41219987 | Common:6; Rare:53 | ||||
| chr19:41220394-41221262 | Common:1; Rare:226 | ||||
| chr19:41262168-41262571 | Rare:70 | ||||
| chr19:41264309-41265301 | Common:6; Rare:267 | ||||
| chr19:41267779-41268098 | Common:1; Rare:53 | ||||
| chr19:41310126-41310308 | Rare:75 | ||||
| chr19:41310378-41310507 | Rare:32 | ||||
| chr19:41342206-41342293 | Rare:22; Clinvar (pathogenic):2 | ||||
| chr19:41350751-41350885 | Common:1; Rare:26 | ||||
| chr19:41353276-41353820 | Common:2; Rare:113 | ||||
| chr19:41353897-41354208 | Rare:88 | ||||
| chr19:41363795-41364001 | Common:1; Rare:75; Clinvar:1 |