| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10568961-10569221 | Common:2; Rare:68 | ||||
| chr19:10587263-10587386 | Common:1; Rare:24 | ||||
| chr19:10653817-10653881 | Rare:27 | ||||
| chr19:10836310-10836571 | Common:2; Rare:66 | ||||
| chr19:10928557-10928812 | Common:2; Rare:77 | ||||
| chr19:11089159-11089499 | Rare:45; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:11155768-11156050 | Common:3; Rare:65 | ||||
| chr19:11197504-11197622 | Common:1; Rare:32 | ||||
| chr19:11355255-11355489 | Common:1; Rare:78 | ||||
| chr19:11419305-11419460 | Rare:32 | ||||
| chr19:11435150-11435694 | Common:7; Rare:164; Clinvar:2; Clinvar (benign):5 | ||||
| chr19:11529086-11529256 | Rare:32 | ||||
| chr19:11559195-11559401 | Common:1; Rare:63 | ||||
| chr19:11597355-11597522 | Rare:53 | ||||
| chr19:11738874-11739110 | Common:4; Rare:74 |