| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26193757-26193919 | Rare:49; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:26227247-26227439 | Rare:39 | ||||
| chr2:26238933-26239111 | Common:1; Rare:42; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:26256218-26256413 | Rare:26 | ||||
| chr2:26298637-26298909 | Common:4; Rare:59 | ||||
| chr2:26299984-26300061 | Rare:20 | ||||
| chr2:26491864-26492155 | Rare:46 | ||||
| chr2:27056416-27056790 | Common:2; Rare:96 | ||||
| chr2:27067114-27067245 | Common:2; Rare:25 | ||||
| chr2:27215483-27215753 | Common:1; Rare:86 | ||||
| chr2:27265038-27265275 | Rare:41 | ||||
| chr2:27321133-27321349 | Common:1; Rare:42 | ||||
| chr2:27324370-27324527 | Common:1; Rare:32 | ||||
| chr2:27382149-27382625 | Rare:88 | ||||
| chr2:27383615-27383915 | Common:1; Rare:66 |