| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:120445097-120445458 | Common:1; Rare:92 | ||||
| chr8:122781249-122781579 | Common:1; Rare:71 | ||||
| chr8:122781582-122781946 | Common:3; Rare:70 | ||||
| chr8:123274339-123274698 | Common:2; Rare:113 | ||||
| chr8:123396359-123396507 | Common:1; Rare:79 | ||||
| chr8:123416323-123416846 | Common:1; Rare:135 | ||||
| chr8:123541006-123541198 | Common:1; Rare:66 | ||||
| chr8:123652908-123653007 | Common:1; Rare:28 | ||||
| chr8:123768319-123768466 | Rare:53 | ||||
| chr8:124372652-124372844 | Common:2; Rare:81 | ||||
| chr8:124474521-124474714 | Common:1; Rare:74 | ||||
| chr8:124474963-124475242 | Rare:101 | ||||
| chr8:124538981-124539287 | Common:2; Rare:157; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124546854-124547103 | Rare:53; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:124728391-124728621 | Rare:71 |