| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48624015-48624410 | Common:1; Rare:98 | ||||
| chr19:48719696-48719769 | Common:1; Rare:12 | ||||
| chr19:48810843-48811128 | Rare:88 | ||||
| chr19:48954596-48954922 | Common:1; Rare:115 | ||||
| chr19:48965240-48965458 | Rare:64; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr19:48993204-48993909 | Common:9; Rare:248; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:49085123-49085541 | Common:3; Rare:169 | ||||
| chr19:49114070-49114402 | Common:4; Rare:85 | ||||
| chr19:49149376-49149501 | Rare:37 | ||||
| chr19:49155181-49155580 | Common:1; Rare:83 | ||||
| chr19:49157529-49157872 | Common:3; Rare:106; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49335301-49335458 | Common:1; Rare:28 | ||||
| chr19:49362367-49362473 | Rare:27 | ||||
| chr19:49453094-49453300 | Common:1; Rare:65 | ||||
| chr19:49487342-49487644 | Common:5; Rare:112 |