| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46120952-46121208 | Common:2; Rare:37 | ||||
| chr11:46121219-46121317 | Rare:18 | ||||
| chr11:46617147-46617588 | Common:5; Rare:125 | ||||
| chr11:46700549-46700830 | Common:1; Rare:72 | ||||
| chr11:46700920-46701083 | Common:3; Rare:47 | ||||
| chr11:46846211-46846412 | Common:1; Rare:55 | ||||
| chr11:47214832-47215110 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47248774-47248944 | Rare:69 | ||||
| chr11:47257790-47258045 | Rare:51 | ||||
| chr11:47268266-47268614 | Common:1; Rare:104; Clinvar (pathogenic):1 | ||||
| chr11:47269556-47269823 | Common:1; Rare:94 | ||||
| chr11:47270011-47270223 | Common:1; Rare:78 | ||||
| chr11:47426406-47426648 | Rare:60 | ||||
| chr11:47565478-47565682 | Common:3; Rare:45 | ||||
| chr11:47578934-47579106 | Rare:91; Clinvar:2; Clinvar (pathogenic):1 |