| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65333624-65333896 | Common:1; Rare:117 | ||||
| chr11:65354524-65354829 | Common:1; Rare:89 | ||||
| chr11:65382636-65382762 | Rare:20 | ||||
| chr11:65386482-65386736 | Common:1; Rare:76 | ||||
| chr11:65524827-65525170 | Rare:63 | ||||
| chr11:65537831-65538132 | Common:1; Rare:108; Clinvar (pathogenic):1 | ||||
| chr11:65540701-65540755 | Common:2; Rare:20 | ||||
| chr11:65570245-65570510 | Rare:94 | ||||
| chr11:65607011-65607328 | Common:3; Rare:106 | ||||
| chr11:65611267-65611420 | Rare:31 | ||||
| chr11:65614186-65614279 | Rare:22 | ||||
| chr11:65615604-65615851 | Common:2; Rare:90 | ||||
| chr11:65638011-65638139 | Common:3; Rare:58 | ||||
| chr11:65662824-65663116 | Common:1; Rare:71 | ||||
| chr11:65712156-65712288 | Rare:48 |