| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:32627912-32628119 | Rare:58 | ||||
| chr2:33476355-33476653 | Common:4; Rare:63 | ||||
| chr2:33599199-33599445 | Common:1; Rare:94 | ||||
| chr2:37084269-37084569 | Common:4; Rare:114 | ||||
| chr2:37231535-37231703 | Common:4; Rare:94; Clinvar (benign):3 | ||||
| chr2:37324698-37324911 | Common:1; Rare:82 | ||||
| chr2:37925415-37925559 | Rare:60 | ||||
| chr2:38073316-38073458 | Rare:25 | ||||
| chr2:38076138-38076282 | Rare:35 | ||||
| chr2:38602855-38603145 | Common:4; Rare:114 | ||||
| chr2:38749664-38749966 | Common:2; Rare:94 | ||||
| chr2:38751296-38751616 | Common:5; Rare:162 | ||||
| chr2:38875886-38876075 | Common:1; Rare:70 | ||||
| chr2:39120995-39121141 | Rare:54 | ||||
| chr2:39124809-39124929 | Rare:24 |