Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:3855551-3855687 | Common:2; Rare:28 | ||||
chr11:4094594-4094906 | Common:2; Rare:87 | ||||
chr11:4608171-4608416 | Common:1; Rare:68 | ||||
chr11:5624903-5625029 | Rare:19 | ||||
chr11:6234621-6234795 | Common:2; Rare:52 | ||||
chr11:6320490-6320573 | Common:2; Rare:25 | ||||
chr11:6390225-6390562 | Common:3; Rare:101; Clinvar (benign):1 | ||||
chr11:6473878-6474130 | Rare:76 | ||||
chr11:6481292-6481558 | Common:5; Rare:123 | ||||
chr11:6603544-6603835 | Common:4; Rare:86; Clinvar (benign):3 | ||||
chr11:6683261-6683652 | Common:6; Rare:148 | ||||
chr11:7020323-7020582 | Common:1; Rare:91 | ||||
chr11:8682623-8682816 | Common:2; Rare:87 | ||||
chr11:8717858-8718184 | Common:7; Rare:83 | ||||
chr11:8964366-8964523 | Common:4; Rare:52 |