| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127290652-127290839 | Rare:40 | ||||
| chr5:127517359-127517714 | Common:7; Rare:133 | ||||
| chr5:129094476-129094778 | Common:3; Rare:128 | ||||
| chr5:131170692-131171002 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr5:131532992-131533087 | Common:1; Rare:15 | ||||
| chr5:131635180-131635398 | Common:1; Rare:84 | ||||
| chr5:131796936-131797246 | Rare:91 | ||||
| chr5:132556813-132557020 | Common:1; Rare:70; Clinvar:1 | ||||
| chr5:132866401-132866694 | Common:1; Rare:94; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:133051851-133052152 | Rare:107 | ||||
| chr5:133968573-133968737 | Rare:64 | ||||
| chr5:134004516-134004869 | Common:2; Rare:121 | ||||
| chr5:134004913-134005018 | Rare:23 | ||||
| chr5:134176934-134177261 | Common:1; Rare:96 | ||||
| chr5:134371025-134371189 | Common:1; Rare:43 |