| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:30147297-30147526 | Rare:77 | ||||
| chr2:30147846-30148014 | Common:2; Rare:57 | ||||
| chr2:30447165-30447413 | Common:3; Rare:78 | ||||
| chr2:31138035-31138185 | Common:2; Rare:45 | ||||
| chr2:31233960-31234120 | Rare:45 | ||||
| chr2:32009997-32010157 | Rare:51 | ||||
| chr2:32010566-32010745 | Rare:40 | ||||
| chr2:32010944-32011129 | Rare:54 | ||||
| chr2:32039761-32039862 | Rare:31 | ||||
| chr2:32064149-32064185 | Rare:10; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:32165730-32165920 | Common:1; Rare:77 | ||||
| chr2:32277701-32277986 | Common:1; Rare:65 | ||||
| chr2:32574959-32575198 | Common:2; Rare:50 | ||||
| chr2:32628014-32628147 | Rare:44 | ||||
| chr2:33599181-33599628 | Common:1; Rare:159 |