| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27370249-27370674 | Common:1; Rare:172 | ||||
| chr2:27380970-27381255 | Rare:60 | ||||
| chr2:27409372-27409789 | Rare:140 | ||||
| chr2:27489696-27489996 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr2:27582987-27583128 | Rare:52 | ||||
| chr2:27628977-27629127 | Common:1; Rare:85 | ||||
| chr2:27663342-27663929 | Rare:185 | ||||
| chr2:27771641-27772029 | Common:1; Rare:121 | ||||
| chr2:27890380-27890829 | Common:1; Rare:118 | ||||
| chr2:28392610-28392858 | Rare:87 | ||||
| chr2:28751524-28752175 | Common:4; Rare:253 | ||||
| chr2:28810704-28810841 | Common:1; Rare:29 | ||||
| chr2:28870221-28870484 | Rare:116 | ||||
| chr2:28894422-28894898 | Common:5; Rare:194 | ||||
| chr2:29115347-29115653 | Common:1; Rare:80 |