| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174395623-174395863 | Common:2; Rare:80 | ||||
| chr2:174486938-174487408 | Common:2; Rare:114 | ||||
| chr2:175168236-175168593 | Common:2; Rare:89 | ||||
| chr2:175181624-175181779 | Common:4; Rare:64 | ||||
| chr2:176002225-176002420 | Common:3; Rare:83 | ||||
| chr2:176269369-176269694 | Common:3; Rare:117 | ||||
| chr2:177212416-177212809 | Common:4; Rare:160 | ||||
| chr2:177263486-177263687 | Common:1; Rare:52 | ||||
| chr2:177392615-177393064 | Common:4; Rare:150; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552750-177553108 | Common:5; Rare:112 | ||||
| chr2:177618706-177619023 | Common:7; Rare:88 | ||||
| chr2:178450731-178451024 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:178451083-178451315 | Common:5; Rare:69; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478495-178478677 | Common:1; Rare:58 | ||||
| chr2:178479985-178480155 | Rare:32 |