| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322483-18322631 | Common:2; Rare:64 | ||||
| chr11:18526851-18526977 | Rare:60 | ||||
| chr11:18588672-18588815 | Rare:50 | ||||
| chr11:18634326-18634584 | Common:2; Rare:82 | ||||
| chr11:18698693-18698747 | Rare:10 | ||||
| chr11:18791784-18791976 | Common:1; Rare:64 | ||||
| chr11:20363657-20363731 | Common:1; Rare:15 | ||||
| chr11:20387481-20387716 | Common:5; Rare:73 | ||||
| chr11:22625808-22626011 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:26994090-26994168 | Common:1; Rare:11 | ||||
| chr11:27363113-27363316 | Rare:87 | ||||
| chr11:27506721-27506864 | Common:1; Rare:66 | ||||
| chr11:28108104-28108406 | Common:1; Rare:89 | ||||
| chr11:30322971-30323183 | Common:2; Rare:61 | ||||
| chr11:30583964-30584136 | Rare:43 |