| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65570156-65570673 | Common:6; Rare:383 | ||||
| chr11:65572090-65572740 | Common:2; Rare:334 | ||||
| chr11:65575789-65576130 | Common:6; Rare:207 | ||||
| chr11:65580802-65581202 | Common:2; Rare:210 | ||||
| chr11:65614038-65614484 | Rare:248 | ||||
| chr11:65615315-65615900 | Common:7; Rare:514 | ||||
| chr11:65615996-65616236 | Rare:181 | ||||
| chr11:65662147-65662800 | Common:3; Rare:230 | ||||
| chr11:65662808-65663475 | Common:14; Rare:388 | ||||
| chr11:65663447-65664033 | Common:6; Rare:143 | ||||
| chr11:65711820-65712339 | Common:2; Rare:402 | ||||
| chr11:65712400-65712791 | Common:4; Rare:179 | ||||
| chr11:65720694-65720853 | Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:65780500-65780705 | Common:1; Rare:64 | ||||
| chr11:65780734-65781099 | Common:3; Rare:292 |