| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32091245-32091448 | Rare:68 | ||||
| chr11:32583673-32583899 | Rare:85 | ||||
| chr11:32892995-32893294 | Common:2; Rare:74 | ||||
| chr11:33015807-33015909 | Rare:36 | ||||
| chr11:33039433-33039795 | Common:1; Rare:89 | ||||
| chr11:33161299-33161674 | Common:7; Rare:99 | ||||
| chr11:33257217-33257439 | Common:3; Rare:77 | ||||
| chr11:33736384-33736605 | Common:2; Rare:68 | ||||
| chr11:33774461-33774690 | Common:2; Rare:86 | ||||
| chr11:34051658-34051771 | Rare:49 | ||||
| chr11:34051978-34052499 | Common:5; Rare:224 | ||||
| chr11:34438766-34438995 | Common:2; Rare:74; Clinvar (benign):1 | ||||
| chr11:34916242-34916618 | Common:9; Rare:151; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr11:35138678-35138906 | Common:2; Rare:50 | ||||
| chr11:35139054-35139375 | Rare:88 |