| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11435168-11435440 | Common:2; Rare:71 | ||||
| chr19:11435534-11435707 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:11529086-11529287 | Rare:39 | ||||
| chr19:11539795-11540005 | Common:1; Rare:42 | ||||
| chr19:11559189-11559407 | Common:1; Rare:68 | ||||
| chr19:11597185-11597539 | Common:4; Rare:110 | ||||
| chr19:11738841-11739252 | Common:4; Rare:110 | ||||
| chr19:11766863-11767175 | Common:1; Rare:80 | ||||
| chr19:11798423-11798608 | Common:1; Rare:40 | ||||
| chr19:11814164-11814321 | Common:1; Rare:41 | ||||
| chr19:11848605-11848773 | Common:1; Rare:47 | ||||
| chr19:11887676-11887835 | Common:1; Rare:47 | ||||
| chr19:11924961-11925138 | Common:6; Rare:48 | ||||
| chr19:11964910-11965068 | Common:1; Rare:40 | ||||
| chr19:12035643-12035783 | Common:1; Rare:54 |