| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46700998-46701077 | Common:1; Rare:30 | ||||
| chr11:46846211-46846412 | Common:1; Rare:55 | ||||
| chr11:47176846-47177161 | Common:1; Rare:129 | ||||
| chr11:47183009-47183156 | Rare:29 | ||||
| chr11:47185347-47185621 | Common:2; Rare:54 | ||||
| chr11:47186347-47186529 | Rare:52 | ||||
| chr11:47214315-47214499 | Common:1; Rare:21 | ||||
| chr11:47214837-47215011 | Common:1; Rare:43 | ||||
| chr11:47248791-47248957 | Rare:69 | ||||
| chr11:47269568-47269838 | Common:1; Rare:93 | ||||
| chr11:47269980-47270212 | Common:1; Rare:83 | ||||
| chr11:47426412-47426648 | Rare:57 | ||||
| chr11:47565440-47565625 | Common:3; Rare:34 | ||||
| chr11:47578959-47579106 | Rare:74; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642461-47642779 | Rare:121 |