| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:86337312-86337505 | Common:4; Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:86337578-86337684 | Rare:35 | ||||
| chr2:86440653-86440969 | Common:3; Rare:103 | ||||
| chr2:86441121-86441529 | Common:2; Rare:156 | ||||
| chr2:86442166-86442375 | Rare:68 | ||||
| chr2:86442745-86442794 | Rare:10 | ||||
| chr2:86562115-86562245 | Rare:22 | ||||
| chr2:86562727-86562861 | Rare:37 | ||||
| chr2:86562864-86563102 | Rare:89 | ||||
| chr2:86563104-86563290 | Rare:72 | ||||
| chr2:86563295-86563617 | Common:4; Rare:117 | ||||
| chr2:86622563-86622602 | Rare:8 | ||||
| chr2:86622692-86622912 | Common:1; Rare:61 | ||||
| chr2:86622987-86623099 | Rare:33 | ||||
| chr2:86623244-86623676 | Common:2; Rare:99 |