| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:66002134-66002532 | Common:3; Rare:107; Clinvar:3; Clinvar (benign):3 | ||||
| chr11:66011817-66012047 | Common:1; Rare:59 | ||||
| chr11:66257618-66257769 | Rare:37 | ||||
| chr11:66480226-66480448 | Common:1; Rare:59 | ||||
| chr11:66616422-66616636 | Common:1; Rare:56 | ||||
| chr11:66638417-66638751 | Common:4; Rare:141 | ||||
| chr11:66677769-66678096 | Common:1; Rare:118 | ||||
| chr11:66744678-66744885 | Common:2; Rare:83 | ||||
| chr11:67353518-67353779 | Common:2; Rare:70 | ||||
| chr11:67401778-67402053 | Common:2; Rare:103 | ||||
| chr11:68030381-68030733 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:68038910-68039060 | Rare:45; Clinvar:1 | ||||
| chr11:68271895-68272102 | Common:2; Rare:89 | ||||
| chr11:68903784-68903943 | Common:4; Rare:76; Clinvar (benign):6 | ||||
| chr11:69640972-69641195 | Rare:48 |