| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26244598-26244972 | Common:2; Rare:135; Clinvar:5; Clinvar (benign):7 | ||||
| chr2:26345812-26346165 | Common:1; Rare:106 | ||||
| chr2:26764230-26764325 | Rare:38 | ||||
| chr2:27051546-27051681 | Rare:40 | ||||
| chr2:27078511-27078755 | Common:2; Rare:66 | ||||
| chr2:27211920-27212012 | Common:3; Rare:38 | ||||
| chr2:27212225-27212371 | Common:1; Rare:77 | ||||
| chr2:27217218-27217494 | Rare:104 | ||||
| chr2:27323051-27323136 | Rare:20; Clinvar (benign):1 | ||||
| chr2:27356745-27357087 | Rare:95 | ||||
| chr2:27370310-27370641 | Common:1; Rare:131 | ||||
| chr2:27489683-27490006 | Common:1; Rare:80; Clinvar (benign):1 | ||||
| chr2:27582997-27583101 | Rare:40 | ||||
| chr2:27628955-27629069 | Common:1; Rare:55 | ||||
| chr2:27663361-27663432 | Rare:21 |