| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:219176302-219176429 | Common:2; Rare:39 | ||||
| chr2:219176888-219177329 | Common:6; Rare:117 | ||||
| chr2:219178020-219178289 | Common:8; Rare:121 | ||||
| chr2:219178556-219178697 | Rare:40 | ||||
| chr2:219206604-219206940 | Rare:122 | ||||
| chr2:219207023-219207267 | Common:3; Rare:73 | ||||
| chr2:219217912-219218050 | Rare:20 | ||||
| chr2:219218410-219218570 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
| chr2:219218837-219219180 | Common:2; Rare:108 | ||||
| chr2:219229270-219229398 | Common:1; Rare:33 | ||||
| chr2:219229540-219229965 | Common:3; Rare:125 | ||||
| chr2:219230275-219230421 | Rare:61 | ||||
| chr2:219245289-219245588 | Common:2; Rare:83 | ||||
| chr2:219252951-219253062 | Common:1; Rare:29 | ||||
| chr2:219253831-219254114 | Common:2; Rare:84 |