Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65662890-65663010 | Common:1; Rare:33 | ||||
chr11:65711869-65712018 | Rare:47 | ||||
chr11:65712198-65712270 | Rare:26 | ||||
chr11:65856951-65857097 | Common:4; Rare:48 | ||||
chr11:65860172-65860452 | Common:1; Rare:91 | ||||
chr11:65860491-65860754 | Common:1; Rare:81 | ||||
chr11:65872701-65872985 | Common:2; Rare:71; Clinvar:1; Clinvar (benign):2 | ||||
chr11:65888426-65888686 | Common:1; Rare:90 | ||||
chr11:66002122-66002818 | Common:4; Rare:196; Clinvar:3; Clinvar (benign):3 | ||||
chr11:66268400-66268674 | Common:3; Rare:81 | ||||
chr11:66288992-66289418 | Common:1; Rare:109 | ||||
chr11:66347622-66347845 | Common:5; Rare:53 | ||||
chr11:66480220-66480450 | Common:3; Rare:61 | ||||
chr11:66593044-66593232 | Common:1; Rare:66 | ||||
chr11:66616383-66616641 | Common:1; Rare:74 |