| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123416521-123416821 | Rare:81 | ||||
| chr8:124474527-124474714 | Rare:72 | ||||
| chr8:124539037-124539287 | Common:2; Rare:123; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124728400-124728767 | Common:5; Rare:112 | ||||
| chr8:124998188-124998684 | Common:4; Rare:197 | ||||
| chr8:125091731-125091916 | Common:2; Rare:62; Clinvar (benign):2 | ||||
| chr8:126558362-126558628 | Common:1; Rare:100 | ||||
| chr8:127735866-127736076 | Rare:45 | ||||
| chr8:129939646-129939856 | Rare:78 | ||||
| chr8:130016390-130016742 | Common:3; Rare:100 | ||||
| chr8:132675529-132675683 | Rare:45 | ||||
| chr8:133102572-133102722 | Rare:26 | ||||
| chr8:133102757-133102886 | Common:2; Rare:25 | ||||
| chr8:133297233-133297488 | Common:3; Rare:103; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:133571817-133572241 | Rare:106 |