| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:177392672-177393059 | Common:2; Rare:136; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552760-177552855 | Common:1; Rare:32 | ||||
| chr2:177618699-177619023 | Common:7; Rare:92 | ||||
| chr2:178451090-178451325 | Common:5; Rare:72; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478495-178478721 | Common:1; Rare:74 | ||||
| chr2:179264503-179264850 | Common:3; Rare:130 | ||||
| chr2:180007080-180007129 | Rare:9 | ||||
| chr2:180980263-180980545 | Common:1; Rare:88 | ||||
| chr2:182716141-182716345 | Common:2; Rare:73 | ||||
| chr2:183124252-183124443 | Common:4; Rare:62 | ||||
| chr2:186485981-186486360 | Common:3; Rare:108 | ||||
| chr2:186589857-186590034 | Rare:47 | ||||
| chr2:186590193-186590361 | Rare:50 | ||||
| chr2:188291578-188292060 | Common:6; Rare:137 | ||||
| chr2:188292718-188292869 | Common:1; Rare:40 |