| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25380138-25380269 | Rare:29 | ||||
| chr2:25672926-25673103 | Common:1; Rare:44 | ||||
| chr2:25673449-25673835 | Common:1; Rare:139 | ||||
| chr2:25878366-25878795 | Common:5; Rare:122 | ||||
| chr2:25982457-25982614 | Common:1; Rare:38 | ||||
| chr2:26033718-26034296 | Common:5; Rare:209 | ||||
| chr2:26184699-26185093 | Common:2; Rare:93 | ||||
| chr2:26185195-26185265 | Rare:24 | ||||
| chr2:26244276-26244419 | Rare:27 | ||||
| chr2:26244533-26245019 | Common:2; Rare:171; Clinvar:7; Clinvar (benign):9 | ||||
| chr2:26345694-26346203 | Common:2; Rare:146 | ||||
| chr2:26764079-26764389 | Common:4; Rare:104 | ||||
| chr2:26785698-26786159 | Rare:116 | ||||
| chr2:27032753-27033016 | Rare:86 | ||||
| chr2:27050357-27050813 | Common:4; Rare:149 |