| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:124673695-124673934 | Common:4; Rare:77 | ||||
| chr11:124762251-124762424 | Rare:45 | ||||
| chr11:124800406-124800481 | Rare:30 | ||||
| chr11:124954029-124954159 | Common:3; Rare:35 | ||||
| chr11:125063124-125063376 | Common:3; Rare:71 | ||||
| chr11:125111855-125111996 | Common:2; Rare:24 | ||||
| chr11:125164558-125164754 | Rare:37 | ||||
| chr11:125592506-125592930 | Common:6; Rare:137 | ||||
| chr11:125625827-125625943 | Common:3; Rare:45 | ||||
| chr11:125887513-125887742 | Common:2; Rare:69 | ||||
| chr11:125903183-125903328 | Rare:34 | ||||
| chr11:126211613-126211822 | Rare:98 | ||||
| chr11:126264189-126264562 | Rare:112 | ||||
| chr11:126268724-126269207 | Common:2; Rare:185; Clinvar:2; Clinvar (benign):4 | ||||
| chr11:126282971-126283140 | Common:1; Rare:59 |