| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46846211-46846416 | Common:1; Rare:58 | ||||
| chr11:47176837-47177149 | Common:1; Rare:129 | ||||
| chr11:47185354-47185568 | Common:2; Rare:49 | ||||
| chr11:47214367-47214496 | Rare:12 | ||||
| chr11:47214840-47215123 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47234553-47234923 | Rare:106; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47248759-47248959 | Common:1; Rare:81 | ||||
| chr11:47257571-47257749 | Rare:25 | ||||
| chr11:47269531-47269830 | Common:1; Rare:104 | ||||
| chr11:47269972-47270224 | Common:2; Rare:89 | ||||
| chr11:47426402-47426609 | Common:1; Rare:51 | ||||
| chr11:47426884-47426984 | Common:1; Rare:20 | ||||
| chr11:47553024-47553341 | Common:2; Rare:116 | ||||
| chr11:47565460-47565650 | Common:3; Rare:38 | ||||
| chr11:47578945-47579114 | Rare:88; Clinvar:2; Clinvar (pathogenic):1 |