| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:111602207-111602544 | Common:1; Rare:113 | ||||
| chr11:111766363-111766415 | Rare:27 | ||||
| chr11:111871259-111871342 | Rare:22 | ||||
| chr11:111871500-111871629 | Rare:55; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:111879054-111879539 | Rare:163 | ||||
| chr11:112025339-112025477 | Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:112074005-112074356 | Common:1; Rare:73 | ||||
| chr11:112086721-112086905 | Rare:76; Clinvar:1 | ||||
| chr11:112226319-112226691 | Common:1; Rare:152; Clinvar:1; Clinvar (pathogenic):3 | ||||
| chr11:113773668-113773842 | Common:1; Rare:54 | ||||
| chr11:113875503-113875771 | Common:4; Rare:99 | ||||
| chr11:114400421-114400753 | Common:2; Rare:132 | ||||
| chr11:114439293-114439546 | Common:1; Rare:82 | ||||
| chr11:115504390-115504673 | Common:1; Rare:82 | ||||
| chr11:116772971-116773079 | Rare:37 |