| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401778-67402076 | Common:3; Rare:111 | ||||
| chr11:67428300-67428537 | Rare:82 | ||||
| chr11:67443441-67443598 | Common:1; Rare:57 | ||||
| chr11:67469228-67469407 | Common:1; Rare:52 | ||||
| chr11:67482913-67483161 | Rare:56; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67508044-67508211 | Common:1; Rare:52 | ||||
| chr11:67508621-67508768 | Common:3; Rare:53 | ||||
| chr11:67583637-67583864 | Common:1; Rare:75 | ||||
| chr11:68030381-68030744 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038915-68039060 | Rare:43; Clinvar:1 | ||||
| chr11:68213535-68213931 | Common:1; Rare:227 | ||||
| chr11:68271865-68272109 | Common:2; Rare:99 | ||||
| chr11:68460538-68460773 | Common:3; Rare:91 | ||||
| chr11:68903734-68903955 | Common:5; Rare:97; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:69048757-69048993 | Common:6; Rare:89 |