| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:43358802-43359057 | Rare:111 | ||||
| chr11:43359139-43359258 | Rare:42 | ||||
| chr11:43880701-43880935 | Common:2; Rare:65 | ||||
| chr11:44066106-44066349 | Common:3; Rare:61 | ||||
| chr11:45804993-45805193 | Common:3; Rare:52; Clinvar:4; Clinvar (benign):1 | ||||
| chr11:45917818-45918132 | Common:1; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:45918792-45918928 | Rare:42 | ||||
| chr11:46120951-46121283 | Common:2; Rare:50 | ||||
| chr11:46593997-46594103 | Common:1; Rare:23 | ||||
| chr11:46617148-46617588 | Common:5; Rare:125 | ||||
| chr11:46700561-46700853 | Common:1; Rare:77 | ||||
| chr11:46700931-46701077 | Common:2; Rare:41 | ||||
| chr11:46846189-46846446 | Common:1; Rare:76 | ||||
| chr11:47176843-47177126 | Common:1; Rare:116 | ||||
| chr11:47186347-47186544 | Rare:56 |