| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:61955037-61955282 | Common:6; Rare:85; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:61967132-61967294 | Common:1; Rare:45 | ||||
| chr11:61967554-61967950 | Common:8; Rare:141; Clinvar:3 | ||||
| chr11:61968153-61968302 | Rare:50 | ||||
| chr11:62123688-62124140 | Common:7; Rare:118 | ||||
| chr11:62124420-62124704 | Common:3; Rare:39 | ||||
| chr11:62337358-62337552 | Common:4; Rare:52 | ||||
| chr11:62545078-62545278 | Rare:33 | ||||
| chr11:62545575-62546056 | Common:1; Rare:109 | ||||
| chr11:62546775-62546940 | Common:1; Rare:51 | ||||
| chr11:62556224-62556422 | Common:1; Rare:33 | ||||
| chr11:62573725-62574333 | Rare:194 | ||||
| chr11:62574577-62574588 | Rare:2 | ||||
| chr11:62591429-62591961 | Rare:179 | ||||
| chr11:62591993-62592205 | Rare:31 |