| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48445866-48446086 | Common:1; Rare:85 | ||||
| chr19:48615179-48615369 | Common:1; Rare:58 | ||||
| chr19:48619123-48619441 | Common:1; Rare:103 | ||||
| chr19:48619448-48619654 | Rare:64 | ||||
| chr19:48811003-48811124 | Rare:42 | ||||
| chr19:48872208-48872487 | Common:2; Rare:101 | ||||
| chr19:48900157-48900372 | Common:1; Rare:69 | ||||
| chr19:48933510-48933699 | Common:3; Rare:52 | ||||
| chr19:48954703-48954948 | Rare:89 | ||||
| chr19:48965240-48965668 | Rare:138; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48965728-48966087 | Common:1; Rare:138; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr19:48993196-48993508 | Common:3; Rare:138; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:48993553-48993923 | Common:5; Rare:96 | ||||
| chr19:49085088-49085585 | Common:3; Rare:191 | ||||
| chr19:49128060-49128304 | Common:2; Rare:72 |