Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:72109925-72110594 | Common:2; Rare:193; Clinvar:6; Clinvar (benign):2 | ||||
chr11:72112090-72112574 | Rare:443 | ||||
chr11:72112580-72113061 | Common:18; Rare:692 | ||||
chr11:72191899-72192299 | Rare:146; Clinvar:6; Clinvar (benign):6 | ||||
chr11:72223066-72223492 | Common:12; Rare:751 | ||||
chr11:72223651-72224417 | Common:15; Rare:767 | ||||
chr11:72224390-72224790 | Common:1; Rare:181 | ||||
chr11:72224695-72224822 | Rare:38 | ||||
chr11:72308620-72309039 | Common:2; Rare:215 | ||||
chr11:72434104-72434853 | Common:23; Rare:733; Clinvar:3; Clinvar (benign):10 | ||||
chr11:72642275-72642682 | Common:6; Rare:228 | ||||
chr11:72642960-72643408 | Common:4; Rare:187 | ||||
chr11:72722186-72722586 | Rare:142 | ||||
chr11:72752286-72752700 | Common:21; Rare:501 | ||||
chr11:72752640-72752910 | Rare:129 |