| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:122845508-122845621 | Common:3; Rare:44 | ||||
| chr5:123511981-123512166 | Common:1; Rare:48 | ||||
| chr5:126595139-126595361 | Common:5; Rare:100; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr5:129094470-129094760 | Common:3; Rare:118 | ||||
| chr5:131165188-131165356 | Rare:65; Clinvar (benign):1 | ||||
| chr5:131170655-131171002 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr5:131263911-131264117 | Rare:76 | ||||
| chr5:131635160-131635416 | Common:1; Rare:98 | ||||
| chr5:131796969-131797215 | Rare:67 | ||||
| chr5:132369602-132369767 | Common:4; Rare:48; Clinvar (benign):1 | ||||
| chr5:132490774-132491020 | Rare:64 | ||||
| chr5:132556813-132557026 | Common:1; Rare:73; Clinvar:1 | ||||
| chr5:132737506-132737639 | Rare:41 | ||||
| chr5:132866428-132866709 | Common:2; Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133026524-133026746 | Common:4; Rare:49 |