| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11089261-11089543 | Rare:55; Clinvar:12; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:11090344-11090579 | Common:2; Rare:62 | ||||
| chr19:11155689-11156062 | Common:3; Rare:99 | ||||
| chr19:11197501-11197628 | Common:1; Rare:32 | ||||
| chr19:11374570-11374732 | Common:1; Rare:52 | ||||
| chr19:11435157-11435440 | Common:2; Rare:72 | ||||
| chr19:11481044-11481156 | Rare:21 | ||||
| chr19:11529073-11529294 | Rare:42 | ||||
| chr19:11559198-11559407 | Common:1; Rare:64 | ||||
| chr19:11738887-11739107 | Common:4; Rare:69 | ||||
| chr19:11814102-11814313 | Common:1; Rare:56 | ||||
| chr19:11848454-11848779 | Common:1; Rare:76 | ||||
| chr19:11887682-11887823 | Common:1; Rare:42 | ||||
| chr19:11924961-11925131 | Common:6; Rare:46 | ||||
| chr19:12156689-12156833 | Common:1; Rare:36 |