| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:11841882-11842086 | Common:1; Rare:68 | ||||
| chr11:12110360-12110686 | Rare:80 | ||||
| chr11:12161245-12161450 | Common:1; Rare:38 | ||||
| chr11:12377474-12377678 | Rare:79 | ||||
| chr11:14262434-14262736 | Common:2; Rare:64 | ||||
| chr11:14643627-14643770 | Common:1; Rare:65 | ||||
| chr11:16738456-16738854 | Common:3; Rare:93 | ||||
| chr11:17077595-17077854 | Common:2; Rare:107 | ||||
| chr11:17207868-17208082 | Common:2; Rare:77 | ||||
| chr11:17276451-17276827 | Common:5; Rare:107; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18322123-18322330 | Common:4; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322491-18322616 | Common:2; Rare:56 | ||||
| chr11:18394216-18394631 | Common:2; Rare:136; Clinvar (benign):1 | ||||
| chr11:18526841-18526977 | Rare:66 | ||||
| chr11:18588672-18588884 | Common:2; Rare:71 |