| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18588661-18588809 | Rare:55 | ||||
| chr11:20363636-20363753 | Common:2; Rare:24 | ||||
| chr11:20387410-20387765 | Common:8; Rare:114 | ||||
| chr11:22625522-22625598 | Rare:38; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:22625813-22625947 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:27506756-27506857 | Common:1; Rare:43 | ||||
| chr11:28108115-28108405 | Common:1; Rare:87 | ||||
| chr11:30322928-30323173 | Common:2; Rare:74 | ||||
| chr11:31369735-31369888 | Rare:47 | ||||
| chr11:31509575-31509790 | Common:1; Rare:67 | ||||
| chr11:33161443-33161678 | Common:6; Rare:65 | ||||
| chr11:33257157-33257409 | Common:2; Rare:86 | ||||
| chr11:33736391-33736553 | Common:2; Rare:54 | ||||
| chr11:33774493-33774685 | Common:2; Rare:67 | ||||
| chr11:34438776-34438998 | Common:2; Rare:74; Clinvar (benign):1 |