| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:13463100-13463341 | Common:1; Rare:83 | ||||
| chr11:14520318-14520448 | Rare:38 | ||||
| chr11:14643620-14643765 | Common:1; Rare:67 | ||||
| chr11:16738466-16738848 | Common:3; Rare:90 | ||||
| chr11:17077583-17077854 | Common:2; Rare:117 | ||||
| chr11:17207905-17208103 | Common:2; Rare:78 | ||||
| chr11:18012886-18013266 | Common:6; Rare:126 | ||||
| chr11:18322128-18322321 | Common:4; Rare:69; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322437-18322645 | Common:2; Rare:80 | ||||
| chr11:18394422-18394633 | Common:1; Rare:82; Clinvar (benign):1 | ||||
| chr11:18526841-18526987 | Rare:72 | ||||
| chr11:18588667-18588879 | Common:2; Rare:72 | ||||
| chr11:18634326-18634566 | Common:2; Rare:76 | ||||
| chr11:18791768-18792012 | Common:1; Rare:87 | ||||
| chr11:20363518-20363777 | Common:3; Rare:49 |