| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46700532-46700830 | Common:1; Rare:75 | ||||
| chr11:46701011-46701086 | Rare:34 | ||||
| chr11:46719080-46719320 | Rare:58 | ||||
| chr11:46846239-46846412 | Common:1; Rare:48 | ||||
| chr11:47186398-47186536 | Rare:40 | ||||
| chr11:47248774-47248941 | Rare:66 | ||||
| chr11:47269513-47269707 | Common:1; Rare:64 | ||||
| chr11:47269978-47270184 | Common:1; Rare:69 | ||||
| chr11:47565460-47565643 | Common:3; Rare:35 | ||||
| chr11:47578959-47579114 | Rare:81; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642443-47642688 | Rare:104 | ||||
| chr11:47848325-47848404 | Rare:38 | ||||
| chr11:57324869-57325169 | Common:2; Rare:98 | ||||
| chr11:57427050-57427257 | Common:1; Rare:64 | ||||
| chr11:57499620-57499843 | Common:1; Rare:66 |