| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48615029-48615368 | Common:2; Rare:100 | ||||
| chr19:48619139-48619435 | Rare:96 | ||||
| chr19:48624116-48624414 | Common:1; Rare:79 | ||||
| chr19:48811017-48811124 | Rare:38 | ||||
| chr19:48900168-48900372 | Common:1; Rare:67 | ||||
| chr19:48965229-48965609 | Rare:117; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993289-48993485 | Common:2; Rare:90; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:49085130-49085492 | Common:3; Rare:145 | ||||
| chr19:49085495-49085608 | Rare:39 | ||||
| chr19:49155394-49155529 | Rare:24 | ||||
| chr19:49157668-49157852 | Rare:57; Clinvar:1 | ||||
| chr19:49335263-49335462 | Common:1; Rare:34 | ||||
| chr19:49362375-49362473 | Rare:27 | ||||
| chr19:49496138-49496470 | Common:1; Rare:114 | ||||
| chr19:49513116-49513403 | Common:1; Rare:68 |