| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:129491622-129492326 | Common:4; Rare:160; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:129502376-129502749 | Common:4; Rare:64; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr6:129514102-129514463 | Common:1; Rare:94; Clinvar:6; Clinvar (benign):2 | ||||
| chr6:129616239-129616586 | Common:1; Rare:76 | ||||
| chr6:131949629-131949856 | Common:1; Rare:28 | ||||
| chr6:133767418-133767702 | Rare:45 | ||||
| chr6:133891629-133891734 | Rare:29 | ||||
| chr6:133895489-133895795 | Common:1; Rare:64 | ||||
| chr6:133896007-133896159 | Rare:38 | ||||
| chr6:134343181-134343334 | Common:2; Rare:30 | ||||
| chr6:135498417-135498434 | Rare:4 | ||||
| chr6:136785335-136785515 | Rare:35 | ||||
| chr6:137218531-137218652 | Common:3; Rare:19 | ||||
| chr6:137868139-137868267 | Rare:23 | ||||
| chr6:138162567-138162777 | Rare:47 |