| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111602143-111602492 | Common:1; Rare:109 | ||||
| chr11:111766338-111766425 | Rare:47 | ||||
| chr11:111871493-111871642 | Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:111879154-111879553 | Common:1; Rare:119 | ||||
| chr11:111911996-111912146 | Common:2; Rare:29 | ||||
| chr11:111912724-111912747 | Rare:3 | ||||
| chr11:111913148-111913276 | Rare:39 | ||||
| chr11:111977092-111977388 | Common:4; Rare:66 | ||||
| chr11:112025339-112025611 | Common:2; Rare:85; Clinvar:1; Clinvar (benign):4 | ||||
| chr11:112074005-112074351 | Common:1; Rare:72 | ||||
| chr11:112086725-112086917 | Rare:80; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr11:112150607-112150726 | Rare:22 | ||||
| chr11:112150937-112151259 | Common:2; Rare:47 | ||||
| chr11:112163961-112164148 | Common:2; Rare:40 | ||||
| chr11:112226304-112226446 | Rare:65 |