| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27051546-27051689 | Rare:43 | ||||
| chr2:27071382-27071888 | Common:2; Rare:159 | ||||
| chr2:27078433-27078852 | Common:4; Rare:101 | ||||
| chr2:27078995-27079029 | Common:1; Rare:13 | ||||
| chr2:27211920-27212065 | Common:3; Rare:59 | ||||
| chr2:27212229-27212425 | Common:2; Rare:107 | ||||
| chr2:27217296-27217539 | Rare:104 | ||||
| chr2:27323043-27323154 | Rare:27; Clinvar (benign):1 | ||||
| chr2:27356177-27356286 | Rare:26 | ||||
| chr2:27356437-27356556 | Rare:51 | ||||
| chr2:27356750-27356854 | Rare:26 | ||||
| chr2:27356970-27357137 | Common:1; Rare:57 | ||||
| chr2:27370306-27370674 | Common:1; Rare:147 | ||||
| chr2:27489686-27489994 | Common:1; Rare:77; Clinvar (benign):1 | ||||
| chr2:27582973-27583101 | Rare:49 |