| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:73760574-73760720 | Common:1; Rare:36 | ||||
| chr11:73876796-73877036 | Common:4; Rare:66 | ||||
| chr11:74170838-74171434 | Common:3; Rare:188 | ||||
| chr11:74493313-74493390 | Rare:32; Clinvar (pathogenic):1 | ||||
| chr11:74949062-74949368 | Common:6; Rare:95 | ||||
| chr11:75351706-75351868 | Common:3; Rare:50 | ||||
| chr11:75562617-75562864 | Common:1; Rare:65 | ||||
| chr11:76381119-76381341 | Common:2; Rare:71 | ||||
| chr11:76444660-76444693 | Rare:8 | ||||
| chr11:77820848-77821237 | Common:1; Rare:112 | ||||
| chr11:78079577-78079673 | Common:2; Rare:31 | ||||
| chr11:78139578-78139805 | Common:3; Rare:90; Clinvar:2 | ||||
| chr11:78188603-78188939 | Common:2; Rare:103 | ||||
| chr11:83071708-83072116 | Common:4; Rare:111 | ||||
| chr11:83193621-83193786 | Common:1; Rare:75 |