| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48900094-48900423 | Common:2; Rare:96 | ||||
| chr19:48954593-48954877 | Common:1; Rare:99 | ||||
| chr19:48955120-48955354 | Common:1; Rare:53 | ||||
| chr19:48965149-48965526 | Rare:113; Clinvar:2; Clinvar (pathogenic):6 | ||||
| chr19:48992719-48992953 | Common:1; Rare:48 | ||||
| chr19:48993167-48993543 | Common:4; Rare:167; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:48993546-48993965 | Common:5; Rare:116 | ||||
| chr19:49085029-49085574 | Common:3; Rare:202 | ||||
| chr19:49085657-49085709 | Rare:18 | ||||
| chr19:49114251-49114411 | Common:1; Rare:41 | ||||
| chr19:49118705-49118897 | Common:2; Rare:86 | ||||
| chr19:49119040-49119162 | Rare:40 | ||||
| chr19:49127979-49128211 | Rare:71 | ||||
| chr19:49335303-49335537 | Common:1; Rare:55 | ||||
| chr19:49335850-49336024 | Rare:50 |