Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:1933719-1934008 | Rare:96; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr11:1938698-1938729 | Rare:6 | ||||
chr11:2137275-2137449 | Rare:41 | ||||
chr11:2138417-2138534 | Rare:17 | ||||
chr11:2138610-2138693 | Rare:18 | ||||
chr11:2140895-2140982 | Rare:20 | ||||
chr11:3797482-3797703 | Rare:87 | ||||
chr11:3855551-3855711 | Common:2; Rare:32 | ||||
chr11:4393651-4393803 | Rare:38 | ||||
chr11:5624903-5625029 | Rare:19 | ||||
chr11:6390322-6390502 | Common:1; Rare:48 | ||||
chr11:6481299-6481545 | Common:4; Rare:109 | ||||
chr11:6603542-6603829 | Common:4; Rare:88; Clinvar (benign):3 | ||||
chr11:6683249-6683412 | Common:2; Rare:85 | ||||
chr11:7020312-7020519 | Rare:76 |