| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:4608171-4608416 | Common:1; Rare:68 | ||||
| chr11:5624883-5625029 | Rare:24 | ||||
| chr11:6234618-6234794 | Common:2; Rare:54 | ||||
| chr11:6319736-6320013 | Rare:74 | ||||
| chr11:6390237-6390517 | Common:2; Rare:82 | ||||
| chr11:6473889-6474053 | Rare:50 | ||||
| chr11:6481302-6481530 | Common:4; Rare:95 | ||||
| chr11:6603542-6603862 | Common:4; Rare:94; Clinvar (benign):3 | ||||
| chr11:6612654-6612722 | Common:1; Rare:12 | ||||
| chr11:6619369-6619560 | Common:3; Rare:62; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr11:6683261-6683652 | Common:6; Rare:148 | ||||
| chr11:7020327-7020469 | Rare:46 | ||||
| chr11:7513612-7513979 | Common:6; Rare:111 | ||||
| chr11:7576850-7577087 | Common:5; Rare:48 | ||||
| chr11:8594145-8594282 | Rare:55 |