| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34438736-34438960 | Common:1; Rare:67 | ||||
| chr11:34916251-34916439 | Common:4; Rare:73; Clinvar:3; Clinvar (benign):4 | ||||
| chr11:46700567-46700818 | Common:1; Rare:64 | ||||
| chr11:46700976-46701082 | Common:1; Rare:39 | ||||
| chr11:46846235-46846421 | Common:1; Rare:54 | ||||
| chr11:47248791-47248947 | Rare:64 | ||||
| chr11:47257495-47257734 | Common:1; Rare:36 | ||||
| chr11:47578965-47579112 | Rare:75; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:57712020-57712624 | Common:10; Rare:200 | ||||
| chr11:59142743-59142916 | Common:1; Rare:32 | ||||
| chr11:60906483-60906790 | Rare:78 | ||||
| chr11:61333038-61333267 | Rare:81 | ||||
| chr11:61361833-61362177 | Common:2; Rare:86; Clinvar:3 | ||||
| chr11:61362223-61362397 | Common:2; Rare:50; Clinvar:7; Clinvar (benign):1 | ||||
| chr11:61429912-61430140 | Common:1; Rare:101; Clinvar (benign):2 |