| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22625817-22626002 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22829779-22830082 | Common:3; Rare:100 | ||||
| chr11:27363071-27363399 | Rare:147 | ||||
| chr11:27506721-27506842 | Common:1; Rare:59 | ||||
| chr11:28108115-28108364 | Rare:72 | ||||
| chr11:30322945-30323156 | Common:1; Rare:60 | ||||
| chr11:31369737-31369887 | Rare:47 | ||||
| chr11:31509567-31509922 | Common:1; Rare:128 | ||||
| chr11:32583652-32583929 | Rare:99 | ||||
| chr11:33015779-33015942 | Common:1; Rare:61 | ||||
| chr11:33161268-33161686 | Common:7; Rare:116 | ||||
| chr11:33257180-33257417 | Common:2; Rare:79 | ||||
| chr11:33736400-33736581 | Common:1; Rare:60 | ||||
| chr11:33774494-33774670 | Common:2; Rare:62 | ||||
| chr11:34053323-34053462 | Rare:36 |