| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27086505-27086810 | Common:4; Rare:94; Clinvar (benign):1 | ||||
| chr2:27134600-27134728 | Rare:57 | ||||
| chr2:27211747-27212173 | Common:4; Rare:151 | ||||
| chr2:27212225-27212398 | Common:2; Rare:96 | ||||
| chr2:27217270-27217544 | Rare:116 | ||||
| chr2:27263021-27263343 | Common:1; Rare:74 | ||||
| chr2:27323029-27323160 | Rare:37; Clinvar (benign):1 | ||||
| chr2:27356177-27356291 | Rare:28 | ||||
| chr2:27356468-27356538 | Rare:30 | ||||
| chr2:27356737-27357221 | Common:2; Rare:146 | ||||
| chr2:27370254-27370657 | Common:1; Rare:166 | ||||
| chr2:27380558-27380817 | Common:2; Rare:103; Clinvar:6 | ||||
| chr2:27409488-27409753 | Rare:89 | ||||
| chr2:27489673-27490006 | Common:1; Rare:84; Clinvar (benign):1 | ||||
| chr2:27582979-27583106 | Rare:47 |