| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178451090-178451369 | Common:6; Rare:83; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478523-178478875 | Common:1; Rare:93 | ||||
| chr2:180980281-180980545 | Common:1; Rare:86 | ||||
| chr2:180980827-180980967 | Rare:31 | ||||
| chr2:181891635-181892281 | Common:6; Rare:256 | ||||
| chr2:182716074-182716412 | Common:3; Rare:117 | ||||
| chr2:182716830-182717055 | Common:1; Rare:45 | ||||
| chr2:183078685-183078792 | Rare:19 | ||||
| chr2:186485884-186486370 | Common:3; Rare:132 | ||||
| chr2:186506539-186506797 | Rare:53 | ||||
| chr2:186590269-186590460 | Rare:75 | ||||
| chr2:187448240-187448407 | Rare:25 | ||||
| chr2:187554299-187554497 | Rare:40 | ||||
| chr2:188291748-188292037 | Common:3; Rare:83 | ||||
| chr2:188292692-188292861 | Common:1; Rare:42 |