| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22192935-22193266 | Common:1; Rare:76; Clinvar:1 | ||||
| chr11:22625483-22625609 | Rare:58; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625808-22626019 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22666508-22666873 | Common:1; Rare:84 | ||||
| chr11:22666940-22667159 | Common:1; Rare:58 | ||||
| chr11:24496891-24497155 | Common:2; Rare:73 | ||||
| chr11:27363064-27363296 | Rare:108 | ||||
| chr11:27506725-27506875 | Common:1; Rare:70 | ||||
| chr11:28108115-28108421 | Common:1; Rare:94 | ||||
| chr11:30016943-30017086 | Rare:35 | ||||
| chr11:30322971-30323202 | Common:2; Rare:65 | ||||
| chr11:30584197-30584456 | Common:17; Rare:45 | ||||
| chr11:31369731-31369902 | Rare:52 | ||||
| chr11:31509566-31509784 | Common:1; Rare:67 | ||||
| chr11:32091007-32091131 | Common:1; Rare:37 |