| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:132675534-132675647 | Rare:32 | ||||
| chr8:133244280-133244391 | Common:2; Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:133297033-133297481 | Common:4; Rare:160; Clinvar:4; Clinvar (benign):2 | ||||
| chr8:133570361-133570583 | Common:1; Rare:50 | ||||
| chr8:133571793-133572251 | Common:1; Rare:119 | ||||
| chr8:134713002-134713151 | Common:1; Rare:46 | ||||
| chr8:140511231-140511569 | Common:3; Rare:131 | ||||
| chr8:140718575-140718895 | Rare:53 | ||||
| chr8:141001124-141001428 | Common:2; Rare:99 | ||||
| chr8:142669952-142670308 | Common:9; Rare:124 | ||||
| chr8:142700305-142700529 | Common:5; Rare:90 | ||||
| chr8:142726984-142727295 | Common:4; Rare:115 | ||||
| chr8:142741801-142742034 | Rare:58; Clinvar (pathogenic):1 | ||||
| chr8:142742328-142742504 | Common:3; Rare:49; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr8:142777304-142777632 | Common:5; Rare:52 |