| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123041750-123041983 | Rare:49 | ||||
| chr8:123042119-123042440 | Common:2; Rare:95 | ||||
| chr8:123072692-123072788 | Rare:26 | ||||
| chr8:123241293-123241444 | Common:1; Rare:68 | ||||
| chr8:123274228-123274711 | Common:2; Rare:131 | ||||
| chr8:123416359-123416826 | Rare:121 | ||||
| chr8:123416955-123417226 | Common:2; Rare:54 | ||||
| chr8:123768328-123768466 | Rare:50 | ||||
| chr8:124450181-124450377 | Common:1; Rare:34 | ||||
| chr8:124450718-124450841 | Common:4; Rare:41 | ||||
| chr8:124474509-124474788 | Common:1; Rare:103 | ||||
| chr8:124474941-124475271 | Rare:117 | ||||
| chr8:124538981-124539286 | Common:2; Rare:157; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124727933-124727961 | Rare:4 | ||||
| chr8:124728373-124728609 | Rare:66 |