| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:22625803-22626015 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr11:27363084-27363331 | Rare:109 | ||||
| chr11:27506711-27506935 | Common:1; Rare:93 | ||||
| chr11:27698964-27699221 | Common:1; Rare:49 | ||||
| chr11:27700380-27700820 | Common:4; Rare:121 | ||||
| chr11:27722050-27722291 | Rare:43 | ||||
| chr11:28107592-28107852 | Common:1; Rare:40 | ||||
| chr11:28108115-28108476 | Common:2; Rare:107 | ||||
| chr11:28110201-28110343 | Rare:34 | ||||
| chr11:30322912-30323176 | Common:2; Rare:77 | ||||
| chr11:31369684-31369963 | Common:1; Rare:78 | ||||
| chr11:31509572-31509957 | Common:1; Rare:142 | ||||
| chr11:31805903-31806303 | Common:6; Rare:174 | ||||
| chr11:31810165-31810565 | Rare:158 | ||||
| chr11:31811231-31811503 | Rare:50; Clinvar:1 |