| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:31816428-31816576 | Rare:37 | ||||
| chr11:31817889-31818085 | Common:2; Rare:54 | ||||
| chr11:32583663-32583914 | Rare:93 | ||||
| chr11:33015838-33015935 | Common:1; Rare:43 | ||||
| chr11:33039945-33039982 | Rare:10 | ||||
| chr11:33161449-33161682 | Common:6; Rare:65 | ||||
| chr11:33257149-33257436 | Common:3; Rare:99 | ||||
| chr11:33736391-33736605 | Common:2; Rare:66 | ||||
| chr11:33774493-33774666 | Common:2; Rare:60 | ||||
| chr11:34105481-34105697 | Common:2; Rare:74 | ||||
| chr11:34438784-34439004 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr11:34916292-34916676 | Common:10; Rare:156; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138954-35139181 | Common:1; Rare:54 | ||||
| chr11:35419037-35419275 | Common:1; Rare:55 | ||||
| chr11:35419546-35419685 | Rare:27 |