Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:59781750-59781837 | Common:1; Rare:12 | ||||
chr11:61313959-61314140 | Rare:58 | ||||
chr11:62444630-62444709 | Rare:19 | ||||
chr11:64247513-64247579 | Rare:13 | ||||
chr11:64294838-64295080 | Common:1; Rare:35 | ||||
chr11:65422651-65422805 | Common:2; Rare:44 | ||||
chr11:65455107-65455290 | Rare:85 | ||||
chr11:65497381-65497772 | Rare:157 | ||||
chr11:65501275-65502186 | Common:2; Rare:415 | ||||
chr11:65526000-65526276 | Rare:94; Clinvar (pathogenic):1 | ||||
chr11:66061696-66061996 | Rare:73 | ||||
chr11:66346493-66346601 | Rare:35; Clinvar (benign):1 | ||||
chr11:66368945-66369107 | Rare:43 | ||||
chr11:67805309-67805617 | Common:3; Rare:109 | ||||
chr11:72608533-72608668 | Rare:22 |