| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123274527-123274814 | Common:2; Rare:82 | ||||
| chr8:123275186-123275586 | Rare:99 | ||||
| chr8:123396362-123396559 | Common:2; Rare:91 | ||||
| chr8:123396564-123396964 | Common:3; Rare:192 | ||||
| chr8:123416637-123416806 | Rare:49 | ||||
| chr8:123416920-123417251 | Common:4; Rare:72 | ||||
| chr8:123768276-123768560 | Common:2; Rare:96 | ||||
| chr8:124372654-124372918 | Common:2; Rare:93 | ||||
| chr8:124450761-124450892 | Common:4; Rare:55 | ||||
| chr8:124474518-124474775 | Common:1; Rare:93 | ||||
| chr8:124538292-124538692 | Common:3; Rare:118 | ||||
| chr8:124539030-124539195 | Common:2; Rare:94; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124727016-124727135 | Rare:35 | ||||
| chr8:124728466-124728631 | Common:2; Rare:50 | ||||
| chr8:124973080-124973510 | Rare:95 |