| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:15073533-15073609 | Common:2; Rare:18 | ||||
| chr11:16612922-16613167 | Common:1; Rare:38 | ||||
| chr11:16738432-16738854 | Common:3; Rare:103 | ||||
| chr11:17014198-17014330 | Rare:47 | ||||
| chr11:17077608-17077968 | Common:2; Rare:149 | ||||
| chr11:17207911-17208149 | Common:2; Rare:89 | ||||
| chr11:17276557-17276818 | Common:3; Rare:73; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:18012889-18013044 | Common:2; Rare:58 | ||||
| chr11:18322128-18322317 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322474-18322656 | Common:2; Rare:73 | ||||
| chr11:18394409-18394630 | Common:1; Rare:87; Clinvar (benign):1 | ||||
| chr11:18396086-18396408 | Common:1; Rare:120 | ||||
| chr11:18526841-18526987 | Rare:72 | ||||
| chr11:18588667-18588815 | Rare:53 | ||||
| chr11:18634317-18634580 | Common:2; Rare:85 |