| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:27506725-27506845 | Common:1; Rare:59 | ||||
| chr11:28108118-28108396 | Common:1; Rare:84 | ||||
| chr11:30322906-30323162 | Common:2; Rare:74 | ||||
| chr11:31369737-31369892 | Rare:47 | ||||
| chr11:31509586-31509784 | Common:1; Rare:62 | ||||
| chr11:32090810-32091148 | Common:3; Rare:100 | ||||
| chr11:33039225-33039620 | Common:1; Rare:106 | ||||
| chr11:33161398-33161657 | Common:6; Rare:67 | ||||
| chr11:33258125-33258346 | Rare:86 | ||||
| chr11:33736391-33736630 | Common:2; Rare:79 | ||||
| chr11:34051626-34051754 | Rare:54 | ||||
| chr11:34052119-34052452 | Common:4; Rare:156 | ||||
| chr11:34105493-34105730 | Common:2; Rare:78 | ||||
| chr11:34438776-34439027 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr11:34439181-34439457 | Common:2; Rare:65 |