| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65546543-65546971 | Common:9; Rare:324; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr11:65550890-65551400 | Common:1; Rare:136 | ||||
| chr11:65553122-65554078 | Common:14; Rare:510; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:65558010-65558570 | Common:7; Rare:318 | ||||
| chr11:65558559-65558990 | Common:10; Rare:127 | ||||
| chr11:65569818-65570218 | Common:2; Rare:194 | ||||
| chr11:65570218-65570673 | Common:6; Rare:777 | ||||
| chr11:65571604-65572717 | Common:6; Rare:605 | ||||
| chr11:65575856-65576130 | Common:15; Rare:344 | ||||
| chr11:65610940-65611340 | Rare:107 | ||||
| chr11:65613790-65614601 | Rare:610 | ||||
| chr11:65614983-65616001 | Common:27; Rare:1844 | ||||
| chr11:65615957-65616382 | Common:2; Rare:462 | ||||
| chr11:65637726-65638283 | Common:29; Rare:777 | ||||
| chr11:65638339-65638739 | Common:2; Rare:98 |