| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:62591489-62591863 | Rare:126 | ||||
| chr11:62621941-62622234 | Common:2; Rare:91 | ||||
| chr11:62646566-62646811 | Common:1; Rare:100; Clinvar (pathogenic):1 | ||||
| chr11:62653262-62653524 | Common:1; Rare:77 | ||||
| chr11:62665052-62665317 | Common:4; Rare:111 | ||||
| chr11:62678864-62679219 | Rare:117 | ||||
| chr11:62706214-62706445 | Common:3; Rare:98; Clinvar (benign):5 | ||||
| chr11:62707343-62707724 | Common:5; Rare:84 | ||||
| chr11:62709501-62709659 | Rare:72 | ||||
| chr11:62727455-62727681 | Rare:87 | ||||
| chr11:62727902-62728210 | Common:7; Rare:83 | ||||
| chr11:62728418-62728561 | Common:1; Rare:86 | ||||
| chr11:62753850-62753958 | Common:1; Rare:45 | ||||
| chr11:62754136-62754438 | Common:2; Rare:71 | ||||
| chr11:62761345-62761634 | Common:1; Rare:84 |