| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10836264-10836551 | Common:2; Rare:72 | ||||
| chr19:10928593-10928792 | Common:1; Rare:51 | ||||
| chr19:10960670-10961172 | Common:6; Rare:192; Clinvar (benign):2 | ||||
| chr19:11155783-11156054 | Common:3; Rare:61 | ||||
| chr19:11197509-11197637 | Common:1; Rare:38 | ||||
| chr19:11559205-11559380 | Common:1; Rare:55 | ||||
| chr19:11738914-11739203 | Common:4; Rare:80 | ||||
| chr19:11766925-11767102 | Rare:46 | ||||
| chr19:11798422-11798589 | Common:1; Rare:35 | ||||
| chr19:11887707-11887857 | Common:1; Rare:41 | ||||
| chr19:11924795-11925138 | Common:6; Rare:79 | ||||
| chr19:11964896-11965048 | Common:1; Rare:41 | ||||
| chr19:12156656-12156848 | Common:1; Rare:47 | ||||
| chr19:12162937-12163127 | Rare:58 | ||||
| chr19:12365615-12365787 | Common:3; Rare:46 |