| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:181656627-181656892 | Common:2; Rare:123; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr2:181656934-181657035 | Rare:47; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:181657103-181657159 | Rare:14 | ||||
| chr2:181680513-181680623 | Rare:20; Clinvar:1 | ||||
| chr2:181891701-181891998 | Common:4; Rare:120 | ||||
| chr2:181892152-181892229 | Common:2; Rare:20 | ||||
| chr2:181892453-181892512 | Common:1; Rare:11 | ||||
| chr2:181892672-181892776 | Rare:35 | ||||
| chr2:182715863-182716128 | Common:1; Rare:83 | ||||
| chr2:182716147-182716377 | Common:2; Rare:79 | ||||
| chr2:183078466-183078849 | Rare:85 | ||||
| chr2:183124227-183124602 | Common:5; Rare:117 | ||||
| chr2:183124629-183124687 | Rare:7 | ||||
| chr2:183124722-183124976 | Common:2; Rare:62 | ||||
| chr2:184598387-184598550 | Common:2; Rare:35 |