| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26244592-26244995 | Common:2; Rare:146; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345819-26346165 | Common:1; Rare:103 | ||||
| chr2:26764191-26764369 | Common:2; Rare:66 | ||||
| chr2:27032867-27033009 | Rare:53 | ||||
| chr2:27051546-27051706 | Rare:49 | ||||
| chr2:27071545-27071888 | Common:1; Rare:103 | ||||
| chr2:27078853-27078964 | Rare:28 | ||||
| chr2:27211775-27212103 | Common:3; Rare:115 | ||||
| chr2:27212247-27212404 | Common:2; Rare:85 | ||||
| chr2:27217115-27217545 | Common:1; Rare:147 | ||||
| chr2:27323040-27323149 | Rare:29; Clinvar (benign):1 | ||||
| chr2:27356750-27357170 | Common:2; Rare:121 | ||||
| chr2:27370254-27370656 | Common:1; Rare:165 | ||||
| chr2:27489669-27489982 | Common:1; Rare:79; Clinvar (benign):1 | ||||
| chr2:27582797-27583101 | Rare:103 |