Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65497463-65497837 | Common:1; Rare:166 | ||||
chr11:65507074-65507171 | Common:2; Rare:28 | ||||
chr11:65526000-65526276 | Rare:94; Clinvar (pathogenic):1 | ||||
chr11:65891380-65891437 | Rare:15 | ||||
chr11:65891620-65891702 | Common:1; Rare:16 | ||||
chr11:65899327-65899499 | Rare:33 | ||||
chr11:65915814-65916029 | Rare:54 | ||||
chr11:66883304-66883488 | Common:2; Rare:35 | ||||
chr11:66892262-66892434 | Rare:32 | ||||
chr11:66906017-66906271 | Common:3; Rare:45 | ||||
chr11:67805264-67805509 | Common:2; Rare:98 | ||||
chr11:68013279-68013463 | Rare:31 | ||||
chr11:68891094-68891385 | Common:1; Rare:67 | ||||
chr11:76752631-76753062 | Common:5; Rare:90 | ||||
chr11:76768598-76768670 | Rare:10 |