Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:130314374-130314525 | Common:1; Rare:53 | ||||
chr11:130314870-130315023 | Common:2; Rare:53 | ||||
chr11:131910307-131910516 | Common:5; Rare:62 | ||||
chr11:131910900-131910989 | Rare:22 | ||||
chr11:133532325-133532543 | Common:2; Rare:50 | ||||
chr11:133532567-133532640 | Rare:18 | ||||
chr11:133956965-133957142 | Common:1; Rare:52 | ||||
chr11:134223911-134224103 | Common:2; Rare:61 | ||||
chr11:134224542-134224717 | Rare:66 | ||||
chr11:134253278-134253592 | Common:2; Rare:106; Clinvar (benign):1 | ||||
chr11:134276028-134276309 | Common:4; Rare:54 | ||||
chr11:134276327-134276594 | Common:5; Rare:76 | ||||
chr11:134276705-134276918 | Common:1; Rare:41 | ||||
chr11:134277186-134277353 | Rare:74 | ||||
chr11:134412203-134412320 | Rare:39 |