| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176637544-176637762 | Common:3; Rare:78 | ||||
| chr2:177215388-177215681 | Common:4; Rare:75 | ||||
| chr2:177239774-177239815 | Rare:3 | ||||
| chr2:177247334-177247524 | Common:4; Rare:53 | ||||
| chr2:177248621-177248712 | Common:1; Rare:20 | ||||
| chr2:177262103-177262394 | Common:2; Rare:37 | ||||
| chr2:178438773-178439058 | Common:1; Rare:60 | ||||
| chr2:178538715-178539071 | Common:3; Rare:101; Clinvar:13; Clinvar (benign):9; Clinvar (pathogenic):3 | ||||
| chr2:178592596-178592769 | Common:1; Rare:44; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr2:178698844-178699063 | Common:6; Rare:65; Clinvar:6; Clinvar (benign):3 | ||||
| chr2:181123906-181123957 | Rare:11 | ||||
| chr2:182866082-182866103 | Rare:9 | ||||
| chr2:182928784-182929131 | Common:1; Rare:65 | ||||
| chr2:185762924-185763204 | Rare:51 | ||||
| chr2:185770072-185770384 | Common:2; Rare:51 |