| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129161017-129161152 | Common:1; Rare:53 | ||||
| chr3:129183774-129184119 | Common:2; Rare:128 | ||||
| chr3:129249549-129249676 | Common:1; Rare:42 | ||||
| chr3:129316279-129316302 | Rare:13 | ||||
| chr3:129439867-129440254 | Common:1; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893552-129893873 | Rare:129 | ||||
| chr3:130893940-130894234 | Common:3; Rare:88 | ||||
| chr3:131026735-131026879 | Common:2; Rare:36 | ||||
| chr3:131381487-131381870 | Common:3; Rare:111 | ||||
| chr3:132659766-132659881 | Common:3; Rare:27 | ||||
| chr3:133661854-133662010 | Rare:35 | ||||
| chr3:134485437-134485766 | Rare:79 | ||||
| chr3:134485957-134486229 | Common:2; Rare:93 | ||||
| chr3:136862032-136862275 | Common:1; Rare:67 | ||||
| chr3:138348251-138348324 | Rare:17 |