| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:85647876-85647990 | Rare:26; Clinvar:2 | ||||
| chr11:86302114-86302475 | Common:2; Rare:83 | ||||
| chr11:86672162-86672278 | Rare:28 | ||||
| chr11:88337723-88337892 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:90223015-90223111 | Common:1; Rare:37 | ||||
| chr11:93661456-93661762 | Common:1; Rare:83 | ||||
| chr11:93741330-93741711 | Common:8; Rare:147 | ||||
| chr11:93784200-93784356 | Common:3; Rare:51 | ||||
| chr11:93784832-93784907 | Rare:18 | ||||
| chr11:94493780-94494049 | Common:5; Rare:81; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:94973535-94973681 | Rare:44 | ||||
| chr11:95067447-95067597 | Rare:67 | ||||
| chr11:95089713-95089882 | Common:3; Rare:69 | ||||
| chr11:95789562-95789887 | Common:3; Rare:145 | ||||
| chr11:95790338-95790717 | Common:3; Rare:149 |