| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178451074-178451378 | Common:6; Rare:89; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478504-178478703 | Common:1; Rare:63 | ||||
| chr2:180980268-180980545 | Common:1; Rare:86 | ||||
| chr2:181457237-181457653 | Common:2; Rare:155 | ||||
| chr2:181457685-181457832 | Rare:58 | ||||
| chr2:181891635-181892049 | Common:4; Rare:170 | ||||
| chr2:182715926-182716339 | Common:3; Rare:141 | ||||
| chr2:183124148-183124439 | Common:5; Rare:76 | ||||
| chr2:186486130-186486370 | Common:3; Rare:84 | ||||
| chr2:186589888-186590034 | Rare:42 | ||||
| chr2:188292692-188292869 | Common:1; Rare:44 | ||||
| chr2:188974508-188974576 | Rare:18; Clinvar (pathogenic):1 | ||||
| chr2:189179701-189179711 | |||||
| chr2:189441100-189441438 | Common:1; Rare:85 | ||||
| chr2:189783965-189784078 | Common:2; Rare:38 |