| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17077618-17077893 | Common:2; Rare:118 | ||||
| chr11:17207920-17208093 | Common:1; Rare:67 | ||||
| chr11:18322131-18322306 | Common:3; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18394472-18394626 | Common:1; Rare:65; Clinvar (benign):1 | ||||
| chr11:18526841-18526970 | Rare:64 | ||||
| chr11:18588672-18588809 | Rare:48 | ||||
| chr11:20387417-20387758 | Common:7; Rare:113 | ||||
| chr11:27506738-27506852 | Common:1; Rare:50 | ||||
| chr11:28108091-28108414 | Common:1; Rare:94 | ||||
| chr11:30322944-30323162 | Common:1; Rare:63 | ||||
| chr11:31369737-31369882 | Rare:45 | ||||
| chr11:31509567-31509784 | Common:1; Rare:67 | ||||
| chr11:33161443-33161678 | Common:6; Rare:65 | ||||
| chr11:33257157-33257427 | Common:3; Rare:92 | ||||
| chr11:33736391-33736605 | Common:2; Rare:66 |