Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65386496-65386715 | Rare:69 | ||||
chr11:65524839-65525132 | Rare:44 | ||||
chr11:65570344-65570510 | Rare:70 | ||||
chr11:65614216-65614453 | Rare:46 | ||||
chr11:65662848-65663019 | Common:1; Rare:43 | ||||
chr11:65663324-65663477 | Common:1; Rare:34 | ||||
chr11:65720482-65720578 | Common:1; Rare:54 | ||||
chr11:65873550-65873791 | Common:3; Rare:78 | ||||
chr11:65888426-65888655 | Common:1; Rare:83 | ||||
chr11:65900405-65900711 | Common:3; Rare:67 | ||||
chr11:65961472-65961764 | Common:1; Rare:95 | ||||
chr11:66002078-66002826 | Common:4; Rare:208; Clinvar:8; Clinvar (benign):3 | ||||
chr11:66268411-66268674 | Common:3; Rare:77 | ||||
chr11:66289041-66289398 | Common:1; Rare:83 | ||||
chr11:66345036-66345219 | Common:1; Rare:53 |