| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:35138954-35139221 | Common:1; Rare:59 | ||||
| chr11:36510252-36510372 | Rare:33 | ||||
| chr11:44066114-44066349 | Common:3; Rare:58 | ||||
| chr11:46120942-46121265 | Common:2; Rare:50 | ||||
| chr11:46380461-46380893 | Common:1; Rare:118 | ||||
| chr11:46700551-46700818 | Common:1; Rare:70 | ||||
| chr11:46846258-46846414 | Common:1; Rare:43 | ||||
| chr11:47248786-47248947 | Rare:66 | ||||
| chr11:47565405-47565622 | Common:3; Rare:39 | ||||
| chr11:47578951-47579112 | Rare:84; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:57426740-57426860 | Rare:18 | ||||
| chr11:57514851-57514954 | Rare:16 | ||||
| chr11:57712175-57712625 | Common:9; Rare:151 | ||||
| chr11:58578095-58578182 | Rare:26 | ||||
| chr11:58905301-58905398 | Common:1; Rare:19 |