| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45584745-45585074 | Common:4; Rare:122; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45639119-45639153 | Rare:14 | ||||
| chr19:45639340-45639522 | Common:2; Rare:53 | ||||
| chr19:45642218-45642351 | Rare:38 | ||||
| chr19:45643690-45643835 | Rare:31 | ||||
| chr19:45668121-45668265 | Common:2; Rare:30 | ||||
| chr19:45677030-45677236 | Common:3; Rare:65 | ||||
| chr19:45677316-45677717 | Common:2; Rare:105 | ||||
| chr19:45677819-45678078 | Rare:83 | ||||
| chr19:45691671-45691711 | Rare:8 | ||||
| chr19:45691820-45692090 | Rare:100 | ||||
| chr19:45692225-45692793 | Common:4; Rare:145 | ||||
| chr19:45692847-45692894 | Rare:15 | ||||
| chr19:45730827-45731152 | Common:1; Rare:73 | ||||
| chr19:45768210-45768379 | Rare:70; Clinvar (benign):2; Clinvar (pathogenic):1 |