Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:3057363-3057521 | Rare:61 | ||||
chr11:3797488-3797815 | Rare:117 | ||||
chr11:3855531-3855810 | Common:2; Rare:56 | ||||
chr11:3856083-3856189 | Rare:39 | ||||
chr11:4094559-4094712 | Common:1; Rare:42 | ||||
chr11:4094737-4094867 | Common:1; Rare:40 | ||||
chr11:4393651-4393817 | Rare:42 | ||||
chr11:5624894-5625029 | Rare:21 | ||||
chr11:6390206-6390616 | Common:3; Rare:128; Clinvar:2; Clinvar (benign):1 | ||||
chr11:6390680-6390827 | Common:6; Rare:76; Clinvar:9; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr11:6390831-6390909 | Rare:27; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr11:6440846-6441169 | Common:2; Rare:79 | ||||
chr11:6481292-6481545 | Common:4; Rare:112 | ||||
chr11:6603481-6603835 | Common:4; Rare:107; Clinvar (benign):3 | ||||
chr11:7020303-7020489 | Rare:64 |