| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35331561-35331802 | Common:3; Rare:45 | ||||
| chr19:35332860-35333117 | Common:2; Rare:61 | ||||
| chr19:35448174-35448292 | Rare:26 | ||||
| chr19:35449319-35449542 | Common:2; Rare:38 | ||||
| chr19:35495389-35495569 | Rare:43 | ||||
| chr19:35510006-35510032 | Rare:5 | ||||
| chr19:35510392-35510552 | Rare:38 | ||||
| chr19:35545409-35545725 | Common:4; Rare:97 | ||||
| chr19:35546151-35546295 | Common:2; Rare:22 | ||||
| chr19:35612574-35612907 | Common:2; Rare:102 | ||||
| chr19:35628655-35629117 | Common:4; Rare:138 | ||||
| chr19:35643452-35643657 | Rare:75 | ||||
| chr19:35643713-35643909 | Common:2; Rare:53 | ||||
| chr19:35648064-35648418 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35712516-35712847 | Common:1; Rare:44 |