| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67583561-67583883 | Common:2; Rare:100 | ||||
| chr11:67584056-67584171 | Common:4; Rare:40 | ||||
| chr11:67611170-67611565 | Common:3; Rare:124; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:67612104-67612403 | Common:3; Rare:109; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:68010119-68010380 | Common:1; Rare:65 | ||||
| chr11:68030381-68030501 | Rare:35 | ||||
| chr11:68030575-68030965 | Common:7; Rare:116; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038904-68039093 | Rare:55; Clinvar:1 | ||||
| chr11:68120831-68120968 | Rare:44 | ||||
| chr11:68121372-68121571 | Common:1; Rare:55 | ||||
| chr11:68271907-68272146 | Common:2; Rare:103 | ||||
| chr11:68460556-68460818 | Common:3; Rare:89 | ||||
| chr11:68903725-68903930 | Common:4; Rare:88; Clinvar (benign):6 | ||||
| chr11:69048743-69048960 | Common:5; Rare:75 | ||||
| chr11:69294080-69294234 | Common:1; Rare:26 |