| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124372672-124372834 | Common:1; Rare:56 | ||||
| chr8:124474557-124474778 | Rare:79 | ||||
| chr8:124474818-124475112 | Common:1; Rare:94 | ||||
| chr8:124539040-124539287 | Common:2; Rare:120; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124728406-124728621 | Rare:66 | ||||
| chr8:125091636-125091914 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:127736055-127736263 | Common:3; Rare:43 | ||||
| chr8:131903920-131904184 | Common:1; Rare:90 | ||||
| chr8:132675523-132675646 | Rare:39 | ||||
| chr8:133571817-133572282 | Rare:119 | ||||
| chr8:134713002-134713152 | Common:1; Rare:46 | ||||
| chr8:140511252-140511604 | Common:2; Rare:133 | ||||
| chr8:141001136-141001428 | Common:2; Rare:96 | ||||
| chr8:141128275-141128710 | Common:5; Rare:135 | ||||
| chr8:141391896-141392073 | Common:1; Rare:60 |