| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:128522391-128522546 | Rare:55 | ||||
| chr11:128693797-128694152 | Common:2; Rare:63 | ||||
| chr11:129895535-129895698 | Common:2; Rare:59 | ||||
| chr11:130002818-130002938 | Rare:23 | ||||
| chr11:130314406-130314518 | Common:1; Rare:37 | ||||
| chr11:130448401-130448652 | Rare:61 | ||||
| chr11:131911280-131911471 | Common:1; Rare:66 | ||||
| chr11:134253292-134253601 | Common:2; Rare:108; Clinvar (benign):1 | ||||
| chr11:134331693-134332012 | Common:10; Rare:69 | ||||
| chr12:389249-389400 | Common:1; Rare:58 | ||||
| chr12:401440-401664 | Rare:61 | ||||
| chr12:610367-610519 | Common:2; Rare:15 | ||||
| chr12:643616-643868 | Common:2; Rare:50 | ||||
| chr12:991101-991266 | Common:1; Rare:63 | ||||
| chr12:1970495-1970848 | Common:1; Rare:53 |