| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124539026-124539193 | Common:2; Rare:95; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124998176-124998646 | Common:4; Rare:190 | ||||
| chr8:125091699-125091930 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:126558353-126558628 | Common:1; Rare:103 | ||||
| chr8:127735804-127736329 | Common:4; Rare:120 | ||||
| chr8:134713029-134713152 | Common:1; Rare:44 | ||||
| chr8:141001144-141001543 | Common:4; Rare:129 | ||||
| chr8:143018380-143018558 | Common:2; Rare:56 | ||||
| chr8:143541424-143541643 | Common:2; Rare:72 | ||||
| chr8:143558262-143558410 | Common:1; Rare:60 | ||||
| chr8:143635893-143636084 | Common:2; Rare:86 | ||||
| chr8:143829299-143829432 | Rare:50 | ||||
| chr8:143939614-143939818 | Common:2; Rare:53 | ||||
| chr8:144060680-144060816 | Rare:41 | ||||
| chr8:144078501-144078749 | Common:1; Rare:78 |