| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174410480-174410494 | Rare:2 | ||||
| chr2:175005185-175005353 | Common:2; Rare:60; Clinvar:1 | ||||
| chr2:175168100-175168559 | Common:2; Rare:122 | ||||
| chr2:176002225-176002435 | Common:4; Rare:86 | ||||
| chr2:176135930-176136250 | Common:2; Rare:78 | ||||
| chr2:176188487-176188678 | Common:1; Rare:75 | ||||
| chr2:176188956-176189081 | Common:2; Rare:38 | ||||
| chr2:177212416-177212831 | Common:4; Rare:166 | ||||
| chr2:177263436-177263673 | Common:1; Rare:53 | ||||
| chr2:177263814-177264142 | Common:2; Rare:88 | ||||
| chr2:177264563-177264828 | Common:2; Rare:76 | ||||
| chr2:177392672-177393064 | Common:2; Rare:138; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552741-177552854 | Common:1; Rare:38 | ||||
| chr2:178072695-178072910 | Rare:53 | ||||
| chr2:178450741-178450905 | Rare:59 |