| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:169828487-169828649 | Common:1; Rare:25 | ||||
| chr2:169888259-169888343 | Common:2; Rare:9 | ||||
| chr2:169918777-169919097 | Common:2; Rare:56 | ||||
| chr2:170061556-170061622 | Rare:9 | ||||
| chr2:170601559-170601662 | Rare:25 | ||||
| chr2:170930394-170930680 | Common:1; Rare:53 | ||||
| chr2:170934703-170934982 | Common:1; Rare:68 | ||||
| chr2:171082754-171082797 | Rare:10 | ||||
| chr2:171133780-171133866 | Common:2; Rare:8 | ||||
| chr2:171324841-171324874 | Rare:4 | ||||
| chr2:171535407-171535476 | Rare:10 | ||||
| chr2:171704361-171704448 | Rare:14 | ||||
| chr2:171725469-171725647 | Common:9; Rare:58; Clinvar (benign):1 | ||||
| chr2:171740530-171740566 | Rare:9 | ||||
| chr2:171749605-171749668 | Rare:7 |