| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45478686-45479303 | Common:4; Rare:233 | ||||
| chr19:45496920-45497290 | Common:3; Rare:105 | ||||
| chr19:45507228-45507496 | Common:1; Rare:67 | ||||
| chr19:45584374-45584626 | Common:1; Rare:89; Clinvar:1 | ||||
| chr19:45584756-45585045 | Common:4; Rare:108; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45615969-45616360 | Common:1; Rare:94 | ||||
| chr19:45639099-45639256 | Rare:36 | ||||
| chr19:45642220-45642351 | Rare:37 | ||||
| chr19:45643692-45643869 | Rare:34 | ||||
| chr19:45667791-45668386 | Common:3; Rare:124 | ||||
| chr19:45691876-45692009 | Rare:58 | ||||
| chr19:45692357-45692708 | Common:1; Rare:80 | ||||
| chr19:45730866-45731067 | Common:1; Rare:43 | ||||
| chr19:45768226-45768425 | Rare:91; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:45769141-45769299 | Rare:44 |