Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65577576-65577868 | Rare:58 | ||||
chr11:65614192-65614279 | Rare:19 | ||||
chr11:65662828-65663269 | Common:3; Rare:107 | ||||
chr11:65860157-65860452 | Common:1; Rare:95 | ||||
chr11:65888426-65888678 | Common:1; Rare:88 | ||||
chr11:65890463-65890749 | Common:4; Rare:90 | ||||
chr11:65900361-65900589 | Common:1; Rare:46 | ||||
chr11:66002045-66002543 | Common:3; Rare:135; Clinvar:8; Clinvar (benign):3 | ||||
chr11:66011913-66012020 | Rare:29 | ||||
chr11:66257623-66257851 | Rare:69 | ||||
chr11:66268444-66268655 | Common:3; Rare:68 | ||||
chr11:66347622-66347845 | Common:5; Rare:53 | ||||
chr11:66480232-66480446 | Common:1; Rare:56 | ||||
chr11:66510551-66510696 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr11:66593066-66593264 | Common:1; Rare:68 |