Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:34052138-34052510 | Common:4; Rare:169 | ||||
chr11:34105473-34105733 | Common:2; Rare:87 | ||||
chr11:34438784-34438987 | Common:1; Rare:68 | ||||
chr11:34916287-34916676 | Common:10; Rare:158; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
chr11:35139018-35139346 | Common:1; Rare:86 | ||||
chr11:35525585-35525816 | Rare:56 | ||||
chr11:35943949-35944119 | Common:2; Rare:61 | ||||
chr11:36455741-36456000 | Rare:54 | ||||
chr11:36510240-36510377 | Rare:39 | ||||
chr11:43358795-43358983 | Rare:92 | ||||
chr11:43880729-43880884 | Common:2; Rare:33 | ||||
chr11:44066074-44066339 | Common:3; Rare:68 | ||||
chr11:45805000-45805180 | Common:3; Rare:42; Clinvar:4; Clinvar (benign):1 | ||||
chr11:46594001-46594114 | Common:1; Rare:23 | ||||
chr11:46617203-46617585 | Common:5; Rare:107 |