| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24793073-24793171 | Rare:50 | ||||
| chr2:24971911-24972170 | Common:1; Rare:81 | ||||
| chr2:25878453-25878742 | Common:3; Rare:88 | ||||
| chr2:26033756-26034188 | Common:4; Rare:162 | ||||
| chr2:26244595-26244975 | Common:2; Rare:140; Clinvar:5; Clinvar (benign):8 | ||||
| chr2:26345785-26346178 | Common:1; Rare:117 | ||||
| chr2:26764201-26764327 | Common:1; Rare:49 | ||||
| chr2:27032867-27032995 | Rare:46 | ||||
| chr2:27071604-27071872 | Common:1; Rare:83 | ||||
| chr2:27078468-27078689 | Common:2; Rare:54 | ||||
| chr2:27086490-27086772 | Common:3; Rare:88 | ||||
| chr2:27211944-27212364 | Common:5; Rare:178 | ||||
| chr2:27217235-27217394 | Rare:59 | ||||
| chr2:27323058-27323149 | Rare:23 | ||||
| chr2:27356750-27357105 | Common:1; Rare:99 |