Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65860157-65860279 | Rare:34 | ||||
chr11:65860338-65860860 | Common:3; Rare:173 | ||||
chr11:65861255-65861329 | Common:1; Rare:24 | ||||
chr11:65862012-65862529 | Common:3; Rare:152 | ||||
chr11:65872687-65872968 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
chr11:65873516-65873727 | Common:3; Rare:67 | ||||
chr11:65888363-65888640 | Common:1; Rare:96 | ||||
chr11:65890106-65890180 | Rare:14 | ||||
chr11:65890531-65890793 | Common:3; Rare:82 | ||||
chr11:65900216-65900554 | Common:4; Rare:77 | ||||
chr11:65900557-65900673 | Common:2; Rare:31 | ||||
chr11:65918962-65919311 | Common:2; Rare:147 | ||||
chr11:65919320-65919552 | Rare:68 | ||||
chr11:65919656-65920175 | Common:1; Rare:176 | ||||
chr11:65920578-65920972 | Common:1; Rare:133 |