| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111299669-111299746 | Common:2; Rare:20 | ||||
| chr11:111766345-111766434 | Common:1; Rare:53 | ||||
| chr11:111871255-111871348 | Rare:26 | ||||
| chr11:111871469-111871630 | Rare:68; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:111879154-111879549 | Common:1; Rare:119 | ||||
| chr11:111911800-111912124 | Common:3; Rare:60 | ||||
| chr11:112025339-112025611 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:112073994-112074361 | Common:1; Rare:77 | ||||
| chr11:112074757-112074850 | Rare:7 | ||||
| chr11:112086700-112086893 | Rare:84 | ||||
| chr11:112163896-112163920 | Rare:3 | ||||
| chr11:112163938-112163985 | Rare:12 | ||||
| chr11:112226205-112226487 | Rare:97 | ||||
| chr11:112227689-112227927 | Common:5; Rare:52 | ||||
| chr11:112228539-112228673 | Rare:50; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):4 |