| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:77820710-77820765 | Rare:20 | ||||
| chr11:77820983-77821148 | Common:1; Rare:45 | ||||
| chr11:77994815-77995046 | Common:1; Rare:56 | ||||
| chr11:78079828-78079952 | Common:1; Rare:39 | ||||
| chr11:78139590-78139779 | Common:3; Rare:76; Clinvar:2 | ||||
| chr11:78574761-78574940 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr11:83071792-83072124 | Common:4; Rare:92 | ||||
| chr11:83156989-83157214 | Common:1; Rare:87 | ||||
| chr11:83193629-83193724 | Common:1; Rare:35 | ||||
| chr11:83285931-83286110 | Common:3; Rare:83 | ||||
| chr11:83286333-83286518 | Rare:47 | ||||
| chr11:85628332-85628620 | Common:7; Rare:91 | ||||
| chr11:85647872-85647994 | Rare:28; Clinvar:2 | ||||
| chr11:85665040-85665399 | Common:1; Rare:114 | ||||
| chr11:86069082-86069177 | Rare:33 |