Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65873550-65873694 | Common:2; Rare:46 | ||||
chr11:65888407-65888678 | Common:1; Rare:95 | ||||
chr11:65890448-65890690 | Common:4; Rare:77 | ||||
chr11:65961492-65961769 | Common:1; Rare:92 | ||||
chr11:66002115-66002393 | Common:3; Rare:83; Clinvar:3; Clinvar (benign):3 | ||||
chr11:66002456-66002812 | Common:1; Rare:100; Clinvar:1 | ||||
chr11:66257436-66257828 | Rare:98 | ||||
chr11:66268361-66268674 | Common:3; Rare:93 | ||||
chr11:66289072-66289355 | Common:1; Rare:70 | ||||
chr11:66347543-66347869 | Common:5; Rare:81; Clinvar (benign):2 | ||||
chr11:66371731-66372024 | Common:1; Rare:76 | ||||
chr11:66372458-66372531 | Rare:15 | ||||
chr11:66480239-66480448 | Common:1; Rare:55 | ||||
chr11:66593078-66593209 | Common:1; Rare:45 | ||||
chr11:66616396-66616638 | Common:1; Rare:65 |