Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:6319741-6320056 | Common:1; Rare:87 | ||||
chr11:6390330-6390595 | Common:2; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
chr11:6419055-6419142 | Common:2; Rare:20 | ||||
chr11:6481245-6481542 | Common:4; Rare:122 | ||||
chr11:6603597-6603860 | Common:2; Rare:79; Clinvar (benign):3 | ||||
chr11:8682641-8682816 | Common:2; Rare:78 | ||||
chr11:8964366-8964531 | Common:4; Rare:53 | ||||
chr11:10304840-10305085 | Common:1; Rare:56 | ||||
chr11:10541144-10541345 | Rare:75 | ||||
chr11:10799309-10799641 | Common:4; Rare:114 | ||||
chr11:10800182-10800574 | Rare:103 | ||||
chr11:10858023-10858242 | Common:2; Rare:64 | ||||
chr11:11841954-11842024 | Common:1; Rare:24 | ||||
chr11:12377455-12377633 | Rare:73 | ||||
chr11:16738475-16738836 | Common:3; Rare:84 |