| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:124748753-124749019 | Common:3; Rare:59 | ||||
| chr5:126371203-126371347 | Common:1; Rare:24 | ||||
| chr5:126595173-126595341 | Common:3; Rare:78; Clinvar:5; Clinvar (benign):8 | ||||
| chr5:127030509-127030736 | Common:2; Rare:54 | ||||
| chr5:127290715-127290796 | Rare:20 | ||||
| chr5:127517502-127517707 | Common:6; Rare:93 | ||||
| chr5:131165189-131165378 | Common:1; Rare:75; Clinvar (benign):1 | ||||
| chr5:131170692-131171002 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr5:131263908-131264117 | Rare:76 | ||||
| chr5:131635160-131635424 | Common:1; Rare:101 | ||||
| chr5:131796928-131797216 | Rare:82 | ||||
| chr5:132257511-132257703 | Common:6; Rare:40 | ||||
| chr5:132369553-132369947 | Common:9; Rare:124; Clinvar:5; Clinvar (benign):5 | ||||
| chr5:132490774-132491051 | Rare:71 | ||||
| chr5:132556885-132557045 | Rare:63; Clinvar:1 |