| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45076456-45076641 | Rare:122 | ||||
| chr19:45079016-45079416 | Common:4; Rare:364 | ||||
| chr19:45079579-45079842 | Common:3; Rare:133 | ||||
| chr19:45091457-45091857 | Common:8; Rare:342 | ||||
| chr19:45092492-45093521 | Common:35; Rare:1153 | ||||
| chr19:45178142-45179388 | Common:48; Rare:1246; Clinvar:9; Clinvar (benign):22 | ||||
| chr19:45179379-45179823 | Common:14; Rare:314; Clinvar:10; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr19:45251037-45252119 | Common:18; Rare:663 | ||||
| chr19:45340530-45340830 | Common:5; Rare:173 | ||||
| chr19:45369899-45370299 | Common:2; Rare:152; Clinvar:4 | ||||
| chr19:45370476-45370876 | Common:15; Rare:628; Clinvar:4 | ||||
| chr19:45404743-45405185 | Rare:101 | ||||
| chr19:45405289-45405560 | Common:2; Rare:55 | ||||
| chr19:45405969-45406204 | Common:4; Rare:110 | ||||
| chr19:45406251-45406806 | Common:22; Rare:745 |