| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:47186408-47186542 | Rare:37 | ||||
| chr11:47214840-47215011 | Common:1; Rare:43 | ||||
| chr11:47248786-47248941 | Rare:62 | ||||
| chr11:47269546-47269707 | Common:1; Rare:55 | ||||
| chr11:47269981-47270166 | Common:1; Rare:61 | ||||
| chr11:47426406-47426658 | Rare:62 | ||||
| chr11:47565478-47565632 | Common:3; Rare:30 | ||||
| chr11:47578947-47579114 | Rare:88; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642462-47642793 | Rare:123 | ||||
| chr11:47848317-47848385 | Rare:37 | ||||
| chr11:57335735-57335953 | Common:4; Rare:49 | ||||
| chr11:57530682-57530843 | Common:1; Rare:41 | ||||
| chr11:57657440-57657773 | Common:4; Rare:86 | ||||
| chr11:57712191-57712630 | Common:9; Rare:148 | ||||
| chr11:57761669-57762002 | Common:2; Rare:60 |