| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:123511982-123512268 | Common:1; Rare:77 | ||||
| chr5:123512407-123512536 | Rare:37 | ||||
| chr5:124748821-124748967 | Common:1; Rare:33 | ||||
| chr5:127073436-127073697 | Common:4; Rare:85 | ||||
| chr5:131165173-131165382 | Common:2; Rare:83; Clinvar (benign):1 | ||||
| chr5:131252944-131253059 | Common:1; Rare:26 | ||||
| chr5:131263891-131264163 | Common:1; Rare:104 | ||||
| chr5:131635180-131635422 | Common:1; Rare:91 | ||||
| chr5:131796967-131797263 | Rare:83 | ||||
| chr5:132410742-132411033 | Common:1; Rare:60 | ||||
| chr5:132490711-132491020 | Common:1; Rare:82 | ||||
| chr5:132556793-132557010 | Common:1; Rare:72; Clinvar:1 | ||||
| chr5:132866435-132866676 | Common:1; Rare:77 | ||||
| chr5:133026523-133026754 | Common:4; Rare:51 | ||||
| chr5:133051638-133052121 | Common:2; Rare:172 |