| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:162344280-162344462 | Common:1; Rare:60 | ||||
| chr2:165794636-165794780 | Common:1; Rare:22 | ||||
| chr2:165953672-165953972 | Common:2; Rare:132; Clinvar:11; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:168456043-168456308 | Common:1; Rare:79 | ||||
| chr2:168456636-168456743 | Rare:39 | ||||
| chr2:168890305-168890630 | Common:2; Rare:75 | ||||
| chr2:169479365-169479556 | Common:3; Rare:71; Clinvar (benign):1 | ||||
| chr2:169573386-169573435 | Rare:5 | ||||
| chr2:169573719-169574024 | Common:2; Rare:82 | ||||
| chr2:169584274-169584412 | Rare:58 | ||||
| chr2:169584557-169584844 | Rare:78 | ||||
| chr2:169585044-169585084 | Common:1; Rare:6 | ||||
| chr2:169694427-169694666 | Common:6; Rare:72 | ||||
| chr2:169694704-169694807 | Rare:31 | ||||
| chr2:169733713-169734063 | Common:2; Rare:96 |