| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:123008722-123009032 | Common:6; Rare:85; Clinvar:4; Clinvar (benign):5 | ||||
| chr10:124092336-124092597 | Common:1; Rare:62 | ||||
| chr10:124092705-124092818 | Rare:28 | ||||
| chr10:124093483-124093695 | Common:2; Rare:36 | ||||
| chr10:124791841-124791938 | Rare:44 | ||||
| chr10:125823200-125823682 | Common:1; Rare:168; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:128047453-128047831 | Common:5; Rare:123 | ||||
| chr10:133276824-133277024 | Rare:50 | ||||
| chr10:133308835-133308972 | Rare:65 | ||||
| chr11:207325-207726 | Common:8; Rare:135 | ||||
| chr11:208662-208857 | Rare:76 | ||||
| chr11:236316-236516 | Common:6; Rare:65 | ||||
| chr11:236707-236997 | Common:3; Rare:78 | ||||
| chr11:320670-320908 | Common:5; Rare:98; Clinvar:1 | ||||
| chr11:407105-407414 | Common:9; Rare:94 |