| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:68216560-68217064 | Common:7; Rare:158 | ||||
| chr11:68313220-68313670 | Common:2; Rare:99 | ||||
| chr11:68342348-68342554 | Common:1; Rare:31 | ||||
| chr11:68342608-68343055 | Common:3; Rare:204 | ||||
| chr11:68343880-68344260 | Common:3; Rare:128 | ||||
| chr11:68354450-68354960 | Common:3; Rare:110 | ||||
| chr11:68380350-68380860 | Common:4; Rare:166 | ||||
| chr11:68763277-68763638 | Common:4; Rare:90 | ||||
| chr11:68840347-68841046 | Common:9; Rare:326 | ||||
| chr11:68905751-68906139 | Common:4; Rare:134; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr11:68972620-68973000 | Rare:58 | ||||
| chr11:68974284-68974444 | Common:1; Rare:37 | ||||
| chr11:69011030-69011350 | Common:3; Rare:132 | ||||
| chr11:69043926-69044621 | Common:7; Rare:339 | ||||
| chr11:69106110-69107000 | Common:5; Rare:365 |