| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33161430-33161638 | Common:6; Rare:58 | ||||
| chr11:33257172-33257468 | Common:3; Rare:100 | ||||
| chr11:33257608-33257876 | Common:1; Rare:65 | ||||
| chr11:33258090-33258393 | Rare:112 | ||||
| chr11:33258419-33258626 | Common:2; Rare:72 | ||||
| chr11:34052116-34052613 | Common:4; Rare:222 | ||||
| chr11:34105478-34105724 | Common:2; Rare:82 | ||||
| chr11:34438784-34439057 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr11:34916282-34916709 | Common:10; Rare:175; Clinvar:8; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139021-35139310 | Common:1; Rare:73 | ||||
| chr11:35943927-35944143 | Common:4; Rare:69 | ||||
| chr11:36289360-36289458 | Rare:44 | ||||
| chr11:36510235-36510372 | Rare:38 | ||||
| chr11:43358839-43358983 | Rare:70 | ||||
| chr11:43880701-43880889 | Common:2; Rare:45 |