| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40605571-40605728 | Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:40605804-40605858 | Rare:10 | ||||
| chr19:40614950-40615255 | Common:10; Rare:92 | ||||
| chr19:40634581-40634602 | Rare:3 | ||||
| chr19:40662942-40663038 | Rare:26 | ||||
| chr19:40663173-40663414 | Common:1; Rare:54 | ||||
| chr19:40777383-40777684 | Common:2; Rare:69 | ||||
| chr19:41090110-41090233 | Common:2; Rare:54 | ||||
| chr19:41109692-41109857 | Common:1; Rare:28 | ||||
| chr19:41110014-41110256 | Common:1; Rare:53 | ||||
| chr19:41225900-41226226 | Common:2; Rare:69 | ||||
| chr19:41263204-41263550 | Rare:70 | ||||
| chr19:41323649-41323846 | Common:3; Rare:47 | ||||
| chr19:41352937-41353168 | Common:4; Rare:70; Clinvar (benign):2 | ||||
| chr19:41374088-41374281 | Rare:41 |