| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:34438776-34439061 | Common:2; Rare:94; Clinvar (benign):1 | ||||
| chr11:34916292-34916676 | Common:10; Rare:156; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139018-35139339 | Common:1; Rare:85 | ||||
| chr11:35943949-35944128 | Common:2; Rare:65 | ||||
| chr11:36289378-36289505 | Common:1; Rare:52 | ||||
| chr11:36350112-36350277 | Common:3; Rare:29 | ||||
| chr11:36375931-36376240 | Common:1; Rare:70 | ||||
| chr11:36377528-36377757 | Common:1; Rare:49 | ||||
| chr11:36510236-36510403 | Rare:56 | ||||
| chr11:43311845-43312096 | Common:2; Rare:84 | ||||
| chr11:43358870-43358983 | Rare:57 | ||||
| chr11:43680416-43680714 | Common:2; Rare:66 | ||||
| chr11:43880743-43880905 | Common:2; Rare:40 | ||||
| chr11:44066406-44066530 | Common:2; Rare:36 | ||||
| chr11:44917755-44917993 | Common:1; Rare:53 |