| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123416310-123416820 | Rare:211 | ||||
| chr8:123541201-123541372 | Common:3; Rare:79 | ||||
| chr8:123768287-123768652 | Common:9; Rare:193 | ||||
| chr8:124372291-124372614 | Common:2; Rare:95 | ||||
| chr8:124372618-124372841 | Common:3; Rare:99 | ||||
| chr8:124450696-124450826 | Common:4; Rare:39 | ||||
| chr8:124473910-124474440 | Common:2; Rare:128 | ||||
| chr8:124474513-124475235 | Common:3; Rare:409 | ||||
| chr8:124538302-124538702 | Common:5; Rare:134 | ||||
| chr8:124538981-124539280 | Common:2; Rare:155; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998164-124998963 | Common:9; Rare:278 | ||||
| chr8:125091587-125091949 | Common:4; Rare:213; Clinvar:2; Clinvar (benign):8 | ||||
| chr8:125429782-125429948 | Common:2; Rare:83 | ||||
| chr8:125430217-125430498 | Common:3; Rare:91 | ||||
| chr8:126558362-126558644 | Common:2; Rare:203 |