| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47565500-47565625 | Common:3; Rare:23 | ||||
| chr11:47578968-47579094 | Rare:64; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642469-47642728 | Rare:104 | ||||
| chr11:57324883-57325164 | Common:1; Rare:94 | ||||
| chr11:57515695-57515810 | Rare:25 | ||||
| chr11:57567612-57567767 | Rare:49 | ||||
| chr11:57597464-57597747 | Rare:64; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:57712175-57712621 | Common:9; Rare:148 | ||||
| chr11:57761576-57761974 | Common:3; Rare:80 | ||||
| chr11:58578101-58578197 | Rare:26 | ||||
| chr11:58578220-58578501 | Common:3; Rare:93 | ||||
| chr11:58578759-58578817 | Rare:20 | ||||
| chr11:59142711-59142945 | Common:1; Rare:42 | ||||
| chr11:60906514-60906776 | Rare:66 | ||||
| chr11:61333028-61333259 | Rare:77 |