| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10304866-10305088 | Common:1; Rare:49 | ||||
| chr11:10541145-10541321 | Rare:66 | ||||
| chr11:10693508-10693629 | Common:1; Rare:37 | ||||
| chr11:10751182-10751295 | Rare:34 | ||||
| chr11:10808709-10808779 | Rare:19 | ||||
| chr11:10808870-10809218 | Common:3; Rare:156 | ||||
| chr11:10858023-10858266 | Common:2; Rare:78 | ||||
| chr11:11841895-11842072 | Common:1; Rare:54 | ||||
| chr11:12377473-12377650 | Rare:72 | ||||
| chr11:13463150-13463391 | Common:1; Rare:90 | ||||
| chr11:14520300-14520498 | Rare:64 | ||||
| chr11:16738456-16738854 | Common:3; Rare:93 | ||||
| chr11:17077556-17077842 | Common:3; Rare:120 | ||||
| chr11:17207910-17208102 | Common:2; Rare:73 | ||||
| chr11:18322123-18322317 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):2 |