Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:94128782-94129177 | Common:3; Rare:132 | ||||
chr11:94493780-94494058 | Common:6; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
chr11:94543905-94543985 | Rare:18 | ||||
chr11:94973530-94973733 | Rare:60 | ||||
chr11:95067452-95067612 | Common:1; Rare:72 | ||||
chr11:95089725-95090047 | Common:3; Rare:121 | ||||
chr11:95230790-95230906 | Rare:31 | ||||
chr11:95231406-95231620 | Common:2; Rare:59 | ||||
chr11:95789478-95789824 | Common:2; Rare:163 | ||||
chr11:95790338-95790694 | Common:3; Rare:139 | ||||
chr11:95923829-95924189 | Common:2; Rare:156; Clinvar:6; Clinvar (benign):5 | ||||
chr11:96342758-96342878 | Rare:22 | ||||
chr11:96343134-96343509 | Common:3; Rare:99 | ||||
chr11:96389850-96390061 | Common:1; Rare:92 | ||||
chr11:101127517-101127763 | Common:3; Rare:106 |