| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:127073457-127073530 | Common:2; Rare:17 | ||||
| chr5:127517513-127517712 | Common:4; Rare:85 | ||||
| chr5:129094562-129094759 | Common:2; Rare:78 | ||||
| chr5:131165201-131165382 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr5:131170692-131171002 | Common:1; Rare:63; Clinvar (benign):1 | ||||
| chr5:131252965-131253065 | Common:1; Rare:21 | ||||
| chr5:131263866-131264133 | Common:2; Rare:102 | ||||
| chr5:131635153-131635639 | Common:1; Rare:170 | ||||
| chr5:131796969-131797266 | Rare:83 | ||||
| chr5:132227806-132228162 | Common:4; Rare:88 | ||||
| chr5:132410709-132411017 | Rare:66 | ||||
| chr5:132419710-132419887 | Common:1; Rare:46 | ||||
| chr5:132490774-132491020 | Rare:64 | ||||
| chr5:132556885-132557037 | Rare:60; Clinvar:1 | ||||
| chr5:132737506-132737695 | Rare:56 |