| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10380487-10380861 | Common:13; Rare:112; Clinvar:5 | ||||
| chr19:10568965-10569296 | Common:2; Rare:82 | ||||
| chr19:10653816-10654393 | Common:5; Rare:246 | ||||
| chr19:10654686-10655121 | Common:6; Rare:176 | ||||
| chr19:10655773-10655824 | Rare:12 | ||||
| chr19:10701356-10701504 | Rare:64 | ||||
| chr19:10836200-10836561 | Common:2; Rare:97 | ||||
| chr19:10928583-10928771 | Common:1; Rare:45 | ||||
| chr19:10960657-10961141 | Common:6; Rare:192; Clinvar (benign):1 | ||||
| chr19:11089287-11089516 | Rare:38; Clinvar:9; Clinvar (pathogenic):1 | ||||
| chr19:11090338-11090579 | Common:2; Rare:64 | ||||
| chr19:11155729-11156038 | Common:3; Rare:80 | ||||
| chr19:11197508-11197637 | Common:1; Rare:39 | ||||
| chr19:11339544-11339764 | Common:3; Rare:48 | ||||
| chr19:11374929-11375236 | Common:1; Rare:79 |