| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9835013-9835347 | Rare:136 | ||||
| chr19:10315975-10316262 | Common:2; Rare:95; Clinvar (benign):5 | ||||
| chr19:10333503-10333701 | Rare:64 | ||||
| chr19:10653817-10653881 | Rare:27 | ||||
| chr19:10836274-10836551 | Common:2; Rare:70 | ||||
| chr19:10928599-10928792 | Common:1; Rare:49 | ||||
| chr19:11089295-11089533 | Rare:44; Clinvar:10; Clinvar (pathogenic):1 | ||||
| chr19:11155795-11156088 | Common:3; Rare:69 | ||||
| chr19:11195945-11196116 | Common:4; Rare:35 | ||||
| chr19:11197504-11197637 | Common:1; Rare:40 | ||||
| chr19:11197792-11197974 | Common:2; Rare:59 | ||||
| chr19:11529086-11529327 | Common:1; Rare:43 | ||||
| chr19:11559184-11559374 | Common:1; Rare:62 | ||||
| chr19:11766889-11767107 | Rare:60 | ||||
| chr19:11887668-11887829 | Common:1; Rare:51 |