Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:57712009-57712630 | Common:10; Rare:207 | ||||
chr11:59142771-59142869 | Rare:16 | ||||
chr11:60873102-60873411 | Rare:112; Clinvar (pathogenic):1 | ||||
chr11:60914101-60914240 | Rare:37 | ||||
chr11:61311817-61312072 | Rare:75 | ||||
chr11:61333026-61333267 | Rare:84 | ||||
chr11:61361809-61361954 | Rare:31 | ||||
chr11:61362158-61362411 | Common:2; Rare:79; Clinvar:8; Clinvar (benign):1 | ||||
chr11:61429390-61429477 | Common:1; Rare:26 | ||||
chr11:61429909-61430169 | Common:1; Rare:116; Clinvar:3; Clinvar (benign):5 | ||||
chr11:61792557-61792961 | Common:6; Rare:116 | ||||
chr11:61828031-61828391 | Common:1; Rare:92 | ||||
chr11:61967432-61967531 | Rare:42 | ||||
chr11:61967542-61967664 | Common:2; Rare:55; Clinvar:3 | ||||
chr11:62123806-62124062 | Common:6; Rare:64 |