| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:133297124-133297488 | Common:3; Rare:140; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133571793-133572251 | Common:1; Rare:119 | ||||
| chr8:134713008-134713152 | Common:1; Rare:46 | ||||
| chr8:140511231-140511533 | Common:3; Rare:119 | ||||
| chr8:140718477-140718895 | Rare:72 | ||||
| chr8:141001124-141001428 | Common:2; Rare:99 | ||||
| chr8:141128275-141128730 | Common:5; Rare:139 | ||||
| chr8:141391881-141392073 | Common:1; Rare:69 | ||||
| chr8:142742404-142742439 | Rare:12 | ||||
| chr8:143018380-143018578 | Common:2; Rare:59 | ||||
| chr8:143212892-143213270 | Common:2; Rare:94 | ||||
| chr8:143541424-143541643 | Common:2; Rare:72 | ||||
| chr8:143553500-143553692 | Common:1; Rare:27 | ||||
| chr8:143557997-143558020 | Rare:5 | ||||
| chr8:143558242-143558411 | Common:1; Rare:63 |