| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22625808-22626011 | Common:3; Rare:70; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:22829357-22829422 | Common:1; Rare:18 | ||||
| chr11:24496933-24497235 | Common:3; Rare:79 | ||||
| chr11:27363022-27363296 | Common:1; Rare:125 | ||||
| chr11:27472729-27472877 | Common:1; Rare:37 | ||||
| chr11:27506738-27506875 | Common:1; Rare:59 | ||||
| chr11:28108148-28108457 | Common:2; Rare:88 | ||||
| chr11:30016898-30017086 | Rare:46 | ||||
| chr11:30322971-30323195 | Common:2; Rare:64 | ||||
| chr11:31369728-31369887 | Rare:49 | ||||
| chr11:31509572-31509787 | Common:1; Rare:65 | ||||
| chr11:33015762-33015923 | Common:2; Rare:62 | ||||
| chr11:33161443-33161657 | Common:6; Rare:57 | ||||
| chr11:33257154-33257435 | Common:3; Rare:97 | ||||
| chr11:33257585-33257876 | Common:1; Rare:71 |