| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17276530-17276827 | Common:5; Rare:85; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:18322131-18322289 | Common:3; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18526885-18526971 | Rare:38 | ||||
| chr11:20387455-20387765 | Common:7; Rare:101 | ||||
| chr11:27506747-27506838 | Common:1; Rare:39 | ||||
| chr11:28108134-28108416 | Common:1; Rare:83 | ||||
| chr11:31509576-31509787 | Common:1; Rare:65 | ||||
| chr11:32583662-32583914 | Rare:93 | ||||
| chr11:33736391-33736605 | Common:2; Rare:66 | ||||
| chr11:34438808-34438977 | Common:1; Rare:54 | ||||
| chr11:34916328-34916661 | Common:10; Rare:133; Clinvar:4; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35139012-35139306 | Common:1; Rare:76 | ||||
| chr11:35943942-35944081 | Common:2; Rare:50 | ||||
| chr11:36510254-36510372 | Rare:33 | ||||
| chr11:43680455-43680777 | Common:1; Rare:80 |