| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66744650-66744873 | Common:3; Rare:92 | ||||
| chr11:66907824-66908058 | Common:2; Rare:31 | ||||
| chr11:67056727-67056929 | Common:1; Rare:59 | ||||
| chr11:67303314-67303582 | Rare:67 | ||||
| chr11:67353467-67353802 | Common:2; Rare:86 | ||||
| chr11:67401768-67402075 | Common:3; Rare:113 | ||||
| chr11:67428336-67428571 | Rare:90 | ||||
| chr11:67443458-67443625 | Common:1; Rare:64 | ||||
| chr11:67469205-67469340 | Rare:47 | ||||
| chr11:67508033-67508195 | Common:1; Rare:53 | ||||
| chr11:67508623-67508795 | Common:3; Rare:65 | ||||
| chr11:68038904-68039101 | Rare:58; Clinvar:1 | ||||
| chr11:68271870-68272171 | Common:2; Rare:126 | ||||
| chr11:68460223-68460309 | Common:2; Rare:46 | ||||
| chr11:68903722-68903955 | Common:5; Rare:102; Clinvar:1; Clinvar (benign):7 |