| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48740556-48740713 | Rare:27 | ||||
| chr19:48753673-48753808 | Common:1; Rare:38 | ||||
| chr19:48810997-48811075 | Rare:31 | ||||
| chr19:48868496-48868723 | Rare:38 | ||||
| chr19:48933538-48933702 | Common:3; Rare:44 | ||||
| chr19:48954735-48954931 | Rare:70 | ||||
| chr19:48965240-48965609 | Rare:115; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48965677-48966164 | Common:3; Rare:171; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr19:48993253-48993508 | Common:2; Rare:116; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:48993740-48993909 | Common:4; Rare:53 | ||||
| chr19:49085128-49085590 | Common:3; Rare:182 | ||||
| chr19:49119112-49119272 | Rare:52 | ||||
| chr19:49335386-49335791 | Common:4; Rare:118 | ||||
| chr19:49336914-49337233 | Rare:101 | ||||
| chr19:49453094-49453318 | Common:1; Rare:70 |