| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:126371283-126371357 | Rare:14 | ||||
| chr5:126595132-126595337 | Common:4; Rare:96; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):3 | ||||
| chr5:127030519-127030709 | Common:2; Rare:43 | ||||
| chr5:127290652-127290852 | Rare:42 | ||||
| chr5:129094553-129094769 | Common:2; Rare:89 | ||||
| chr5:129460093-129460373 | Common:4; Rare:66 | ||||
| chr5:131170698-131171013 | Common:1; Rare:66; Clinvar (benign):2 | ||||
| chr5:131635160-131635424 | Common:1; Rare:101 | ||||
| chr5:131796922-131797197 | Rare:82 | ||||
| chr5:132369564-132369740 | Common:4; Rare:54 | ||||
| chr5:132369892-132369964 | Common:2; Rare:28; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:132490774-132491020 | Rare:64 | ||||
| chr5:132866587-132866694 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:132873576-132873669 | Common:1; Rare:24 | ||||
| chr5:133026533-133026763 | Common:5; Rare:53 |