| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48965665-48965926 | Common:1; Rare:98; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr19:48993234-48993556 | Common:4; Rare:142; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:48993740-48993912 | Common:4; Rare:54 | ||||
| chr19:49085109-49085552 | Common:3; Rare:177 | ||||
| chr19:49114059-49114405 | Common:4; Rare:87 | ||||
| chr19:49119102-49119258 | Rare:48 | ||||
| chr19:49128019-49128248 | Common:2; Rare:69 | ||||
| chr19:49149367-49149576 | Common:1; Rare:75 | ||||
| chr19:49167814-49168024 | Common:8; Rare:71; Clinvar:6; Clinvar (benign):7 | ||||
| chr19:49335404-49335496 | Common:1; Rare:23 | ||||
| chr19:49335633-49335714 | Rare:36 | ||||
| chr19:49451742-49451902 | Common:2; Rare:39 | ||||
| chr19:49451911-49451998 | Common:1; Rare:24 | ||||
| chr19:49453094-49453318 | Common:1; Rare:70 | ||||
| chr19:49453473-49453612 | Rare:39 |