Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:9664622-9664686 | Rare:11 | ||||
chr11:10293840-10293982 | Common:3; Rare:35 | ||||
chr11:10294004-10294106 | Rare:19; Clinvar (pathogenic):1 | ||||
chr11:10294121-10294397 | Common:2; Rare:93; Clinvar:4 | ||||
chr11:10294546-10294746 | Rare:46 | ||||
chr11:10304141-10304294 | Common:1; Rare:21 | ||||
chr11:10304479-10305176 | Common:3; Rare:150 | ||||
chr11:10305491-10305686 | Rare:57 | ||||
chr11:10305777-10305826 | Rare:15 | ||||
chr11:10307781-10308277 | Common:3; Rare:126 | ||||
chr11:10450528-10450668 | Rare:33 | ||||
chr11:10450677-10450919 | Common:2; Rare:60 | ||||
chr11:10450923-10451103 | Common:2; Rare:67 | ||||
chr11:10451129-10451311 | Rare:40 | ||||
chr11:10454979-10455107 | Common:1; Rare:29 |