| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27442215-27442410 | Common:1; Rare:64 | ||||
| chr2:27582809-27583106 | Rare:99 | ||||
| chr2:27628967-27629058 | Common:1; Rare:47 | ||||
| chr2:27663369-27663469 | Rare:28 | ||||
| chr2:27663533-27663911 | Rare:132 | ||||
| chr2:27890380-27890825 | Common:1; Rare:116 | ||||
| chr2:28751704-28752175 | Common:2; Rare:192 | ||||
| chr2:28870256-28870454 | Rare:80 | ||||
| chr2:31414698-31415044 | Common:3; Rare:69; Clinvar (benign):1 | ||||
| chr2:32011006-32011112 | Rare:32 | ||||
| chr2:32039446-32039858 | Rare:112 | ||||
| chr2:32165732-32165898 | Common:1; Rare:63 | ||||
| chr2:32628002-32628125 | Rare:41 | ||||
| chr2:33134452-33134644 | Common:2; Rare:35 | ||||
| chr2:33599222-33599445 | Common:1; Rare:83 |