| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177263436-177263687 | Common:1; Rare:58 | ||||
| chr2:177264563-177264826 | Common:2; Rare:76 | ||||
| chr2:177392672-177393066 | Common:2; Rare:139; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552750-177553068 | Common:4; Rare:97 | ||||
| chr2:178072512-178072860 | Rare:76 | ||||
| chr2:178450731-178450897 | Rare:56 | ||||
| chr2:178451062-178451404 | Common:6; Rare:105; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478538-178478666 | Common:1; Rare:40 | ||||
| chr2:180980263-180980545 | Common:1; Rare:88 | ||||
| chr2:181891541-181892244 | Common:6; Rare:273 | ||||
| chr2:186485966-186486344 | Common:3; Rare:103 | ||||
| chr2:188291716-188291945 | Common:2; Rare:60 | ||||
| chr2:188292677-188292849 | Rare:42 | ||||
| chr2:188293001-188293057 | Rare:6 | ||||
| chr2:189441050-189441433 | Common:2; Rare:105 |