| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66268400-66268655 | Common:3; Rare:75 | ||||
| chr11:66289005-66289393 | Common:1; Rare:95 | ||||
| chr11:66345049-66345186 | Common:1; Rare:38 | ||||
| chr11:66347564-66347898 | Common:5; Rare:81 | ||||
| chr11:66480228-66480450 | Common:1; Rare:58 | ||||
| chr11:66510551-66510687 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:66593053-66593223 | Common:1; Rare:62 | ||||
| chr11:66616396-66616636 | Common:1; Rare:65 | ||||
| chr11:66638393-66638747 | Common:4; Rare:156 | ||||
| chr11:66677767-66678054 | Common:1; Rare:108 | ||||
| chr11:66744645-66744887 | Common:3; Rare:100 | ||||
| chr11:67303378-67303588 | Rare:53 | ||||
| chr11:67317676-67317881 | Rare:42 | ||||
| chr11:67401780-67402076 | Common:3; Rare:111 | ||||
| chr11:67428336-67428531 | Rare:67 |