| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49085086-49085195 | Common:1; Rare:26 | ||||
| chr19:49085389-49085541 | Common:1; Rare:74 | ||||
| chr19:49114267-49114396 | Common:1; Rare:31 | ||||
| chr19:49157694-49157835 | Rare:40; Clinvar:1 | ||||
| chr19:49335387-49335478 | Common:1; Rare:21 | ||||
| chr19:49362380-49362473 | Rare:26 | ||||
| chr19:49453094-49453313 | Common:1; Rare:70 | ||||
| chr19:49453452-49453617 | Rare:55 | ||||
| chr19:49496138-49496476 | Common:1; Rare:116 | ||||
| chr19:49513108-49513421 | Common:1; Rare:71 | ||||
| chr19:49580534-49580692 | Rare:47 | ||||
| chr19:49665590-49666041 | Common:6; Rare:208; Clinvar (pathogenic):1 | ||||
| chr19:49851051-49851150 | Rare:38 | ||||
| chr19:49867518-49867633 | Common:2; Rare:39; Clinvar:1 | ||||
| chr19:49877273-49877742 | Common:1; Rare:125 |