| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9786120-9786242 | Rare:37 | ||||
| chr19:9793147-9793348 | Rare:40 | ||||
| chr19:9818792-9818884 | Rare:37 | ||||
| chr19:9827823-9827982 | Common:1; Rare:58 | ||||
| chr19:10333484-10333709 | Common:1; Rare:78 | ||||
| chr19:10380487-10380798 | Common:11; Rare:92; Clinvar:5 | ||||
| chr19:10654697-10655127 | Common:5; Rare:172 | ||||
| chr19:10836274-10836571 | Common:2; Rare:77 | ||||
| chr19:10960689-10961141 | Common:3; Rare:168; Clinvar (benign):1 | ||||
| chr19:11089269-11089516 | Rare:40; Clinvar:9; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:11197504-11197615 | Rare:27 | ||||
| chr19:11418539-11418618 | Rare:12 | ||||
| chr19:11419287-11419450 | Rare:32 | ||||
| chr19:11538588-11538874 | Common:2; Rare:60 | ||||
| chr19:11559174-11559407 | Common:1; Rare:71 |