| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17207931-17208149 | Common:1; Rare:81 | ||||
| chr11:17276569-17276824 | Common:4; Rare:64; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18322127-18322330 | Common:4; Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322431-18322702 | Common:2; Rare:93 | ||||
| chr11:18394488-18394622 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr11:18526870-18526976 | Rare:49 | ||||
| chr11:18588666-18588839 | Common:2; Rare:57 | ||||
| chr11:22625497-22625597 | Rare:47; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr11:27506734-27506857 | Common:1; Rare:55 | ||||
| chr11:28108142-28108396 | Common:1; Rare:72 | ||||
| chr11:30322944-30323164 | Common:1; Rare:63 | ||||
| chr11:31369728-31369915 | Rare:56 | ||||
| chr11:31509576-31509807 | Common:1; Rare:77 | ||||
| chr11:33774481-33774625 | Common:2; Rare:51 | ||||
| chr11:34916302-34916461 | Common:4; Rare:65; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 |