| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:64284560-64284869 | Common:1; Rare:128 | ||||
| chr11:64285404-64285505 | Common:1; Rare:27 | ||||
| chr11:64317417-64317677 | Common:4; Rare:89 | ||||
| chr11:64317985-64318395 | Common:1; Rare:176 | ||||
| chr11:64340153-64340244 | Rare:17 | ||||
| chr11:64359083-64359247 | Common:1; Rare:39 | ||||
| chr11:64744081-64744247 | Rare:33 | ||||
| chr11:64759878-64760102 | Rare:64; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:64769051-64769287 | Rare:62 | ||||
| chr11:64778752-64778894 | Common:1; Rare:55 | ||||
| chr11:64803152-64803299 | Rare:63 | ||||
| chr11:64854778-64854913 | Rare:43 | ||||
| chr11:64878444-64878884 | Common:4; Rare:161 | ||||
| chr11:64996968-64997138 | Common:2; Rare:22 | ||||
| chr11:65014028-65014264 | Rare:59 |