| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94262259-94262299 | Rare:12 | ||||
| chr8:94262304-94262405 | Rare:27 | ||||
| chr8:94553431-94553763 | Common:3; Rare:120 | ||||
| chr8:94719752-94720095 | Common:3; Rare:104 | ||||
| chr8:94895197-94895342 | Rare:45 | ||||
| chr8:94895689-94895806 | Rare:31 | ||||
| chr8:94949354-94949553 | Common:1; Rare:61 | ||||
| chr8:95024784-95025109 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr8:95268718-95268842 | Common:7; Rare:29 | ||||
| chr8:96235510-96235652 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr8:96261566-96261971 | Common:6; Rare:135 | ||||
| chr8:96493716-96493938 | Common:1; Rare:73 | ||||
| chr8:96493951-96494330 | Common:3; Rare:116 | ||||
| chr8:97644738-97644886 | Rare:47 | ||||
| chr8:98045338-98045666 | Common:3; Rare:98 |