Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:57311450-57311724 | Common:1; Rare:71 | ||||
chr11:57324877-57325183 | Common:1; Rare:101 | ||||
chr11:57426587-57426955 | Common:1; Rare:67 | ||||
chr11:57427593-57427897 | Common:3; Rare:45 | ||||
chr11:57514854-57514974 | Rare:22 | ||||
chr11:57515669-57516021 | Common:2; Rare:62 | ||||
chr11:57530675-57530953 | Common:1; Rare:71 | ||||
chr11:57567597-57567767 | Rare:58 | ||||
chr11:57568211-57568418 | Common:1; Rare:39 | ||||
chr11:57597503-57597731 | Rare:51; Clinvar:4; Clinvar (benign):1 | ||||
chr11:57606187-57606531 | Rare:88 | ||||
chr11:57712163-57712806 | Common:10; Rare:228 | ||||
chr11:57741243-57741736 | Common:3; Rare:199 | ||||
chr11:57761584-57761991 | Common:3; Rare:82 | ||||
chr11:58578059-58578545 | Common:4; Rare:150 |