| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26847824-26848168 | Common:2; Rare:99 | ||||
| chr2:27032816-27033006 | Rare:74 | ||||
| chr2:27050652-27050872 | Common:4; Rare:135 | ||||
| chr2:27051528-27051668 | Rare:42 | ||||
| chr2:27071603-27071891 | Common:1; Rare:90 | ||||
| chr2:27086493-27086810 | Common:4; Rare:96; Clinvar (benign):1 | ||||
| chr2:27134567-27134739 | Rare:81 | ||||
| chr2:27211784-27212096 | Common:3; Rare:106 | ||||
| chr2:27212209-27212456 | Common:2; Rare:125 | ||||
| chr2:27212740-27213166 | Rare:278 | ||||
| chr2:27217265-27217475 | Rare:91 | ||||
| chr2:27323030-27323240 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr2:27356106-27356291 | Rare:51 | ||||
| chr2:27356472-27356572 | Rare:42 | ||||
| chr2:27356734-27357233 | Common:2; Rare:148 |