| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75555876-75556020 | Rare:22 | ||||
| chr2:75690027-75690271 | Common:1; Rare:64 | ||||
| chr2:78309565-78309817 | Common:2; Rare:46 | ||||
| chr2:78618674-78618919 | Common:4; Rare:78 | ||||
| chr2:83104218-83104385 | Common:3; Rare:33 | ||||
| chr2:84320783-84320975 | Rare:37 | ||||
| chr2:84424338-84424654 | Rare:46 | ||||
| chr2:84443058-84443387 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:84961051-84961214 | Rare:25 | ||||
| chr2:84962206-84962255 | Rare:11 | ||||
| chr2:84973850-84973962 | Rare:17 | ||||
| chr2:84988086-84988301 | Rare:49 | ||||
| chr2:84989413-84989453 | Rare:6 | ||||
| chr2:84990202-84990486 | Common:1; Rare:56 | ||||
| chr2:85005790-85006036 | Common:1; Rare:37 |