| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48623983-48624368 | Common:1; Rare:91 | ||||
| chr19:48637657-48637802 | Rare:37 | ||||
| chr19:48646019-48646524 | Common:1; Rare:95 | ||||
| chr19:48810852-48810976 | Rare:30 | ||||
| chr19:48872218-48872449 | Common:2; Rare:79 | ||||
| chr19:48954731-48954922 | Rare:67 | ||||
| chr19:48965209-48965604 | Rare:122; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48965691-48965806 | Rare:38 | ||||
| chr19:48993296-48993576 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49085088-49085492 | Common:3; Rare:156 | ||||
| chr19:49115035-49115131 | Rare:21 | ||||
| chr19:49119080-49119373 | Rare:95 | ||||
| chr19:49157696-49157800 | Rare:28; Clinvar:1 | ||||
| chr19:49362386-49362471 | Rare:23 | ||||
| chr19:49451748-49452002 | Common:3; Rare:66 |