| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10654078-10654393 | Common:4; Rare:146 | ||||
| chr19:10654697-10655098 | Common:5; Rare:165 | ||||
| chr19:10960683-10961085 | Common:3; Rare:162 | ||||
| chr19:11089336-11089499 | Rare:23; Clinvar:6; Clinvar (pathogenic):1 | ||||
| chr19:11155777-11156038 | Common:3; Rare:61 | ||||
| chr19:11197509-11197614 | Rare:25 | ||||
| chr19:11339589-11339764 | Common:2; Rare:42 | ||||
| chr19:11435221-11435440 | Common:1; Rare:57 | ||||
| chr19:11559195-11559399 | Common:1; Rare:61 | ||||
| chr19:11597309-11597553 | Common:1; Rare:75 | ||||
| chr19:11766859-11767097 | Rare:66 | ||||
| chr19:11887672-11887866 | Common:1; Rare:58 | ||||
| chr19:11924977-11925128 | Common:5; Rare:41 | ||||
| chr19:11964910-11965054 | Common:1; Rare:37 | ||||
| chr19:12156717-12156862 | Rare:32 |