| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10541122-10541312 | Common:1; Rare:73 | ||||
| chr11:10751169-10751302 | Rare:40 | ||||
| chr11:10808709-10809204 | Common:3; Rare:192 | ||||
| chr11:10858013-10858260 | Common:3; Rare:81 | ||||
| chr11:11841813-11842077 | Common:3; Rare:90 | ||||
| chr11:12377377-12377645 | Common:1; Rare:100 | ||||
| chr11:13463141-13463341 | Common:1; Rare:71 | ||||
| chr11:16738456-16738776 | Common:3; Rare:70 | ||||
| chr11:17207911-17208082 | Common:2; Rare:65 | ||||
| chr11:18106037-18106312 | Common:2; Rare:83 | ||||
| chr11:18322049-18322321 | Common:4; Rare:97; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322476-18322635 | Common:2; Rare:67 | ||||
| chr11:18394432-18394641 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr11:18526835-18526993 | Rare:78 | ||||
| chr11:18588661-18588831 | Common:2; Rare:60 |