| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:175181629-175181729 | Common:4; Rare:52 | ||||
| chr2:176002229-176002414 | Common:3; Rare:80 | ||||
| chr2:176188491-176188701 | Common:2; Rare:88 | ||||
| chr2:176188927-176189107 | Common:2; Rare:60 | ||||
| chr2:177212449-177212831 | Common:4; Rare:151 | ||||
| chr2:177264618-177264793 | Common:2; Rare:52 | ||||
| chr2:177392672-177393029 | Common:2; Rare:130; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552754-177552841 | Common:1; Rare:31 | ||||
| chr2:178072745-178072884 | Rare:36 | ||||
| chr2:178451090-178451347 | Common:6; Rare:77; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:181458074-181458267 | Common:1; Rare:58 | ||||
| chr2:182715935-182716328 | Common:3; Rare:137 | ||||
| chr2:186485822-186486358 | Common:3; Rare:134 | ||||
| chr2:186589979-186590034 | Rare:11 | ||||
| chr2:186590259-186590443 | Rare:72 |