| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66843332-66843464 | Common:5; Rare:66 | ||||
| chr11:66843576-66843722 | Common:1; Rare:57 | ||||
| chr11:66852817-66852858 | Common:1; Rare:17; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:67056763-67057033 | Common:1; Rare:73 | ||||
| chr11:67119702-67119830 | Rare:36 | ||||
| chr11:67119864-67119990 | Rare:31 | ||||
| chr11:67215657-67215944 | Common:2; Rare:40 | ||||
| chr11:67239423-67239695 | Rare:44 | ||||
| chr11:67289228-67289472 | Common:6; Rare:81 | ||||
| chr11:67317662-67317915 | Rare:55 | ||||
| chr11:67353259-67353418 | Rare:49 | ||||
| chr11:67373576-67373743 | Rare:36 | ||||
| chr11:67401562-67401940 | Common:2; Rare:136 | ||||
| chr11:67428258-67428623 | Common:1; Rare:130 | ||||
| chr11:67443797-67443867 | Rare:15 |