| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67428317-67428531 | Rare:72 | ||||
| chr11:67469212-67469360 | Rare:50 | ||||
| chr11:67482936-67483171 | Rare:53; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr11:67583646-67583847 | Common:1; Rare:65 | ||||
| chr11:68038919-68039069 | Rare:44; Clinvar:1 | ||||
| chr11:68271895-68272018 | Rare:58 | ||||
| chr11:68460533-68460767 | Common:3; Rare:89 | ||||
| chr11:68903784-68903943 | Common:4; Rare:76; Clinvar (benign):6 | ||||
| chr11:69640983-69641235 | Common:1; Rare:53 | ||||
| chr11:70398455-70398596 | Common:1; Rare:46 | ||||
| chr11:70416822-70417116 | Common:3; Rare:95 | ||||
| chr11:71448352-71448644 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:71452987-71453268 | Common:3; Rare:80 | ||||
| chr11:71787312-71787528 | Common:13; Rare:77 | ||||
| chr11:72041846-72042084 | Common:2; Rare:51 |