Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:133336854-133337073 | Common:1; Rare:75 | ||||
chr10:133393980-133394263 | Common:2; Rare:129 | ||||
chr11:207372-207720 | Common:7; Rare:103 | ||||
chr11:208662-208857 | Rare:76 | ||||
chr11:236331-236503 | Common:6; Rare:51 | ||||
chr11:236917-237059 | Common:1; Rare:56 | ||||
chr11:307579-307790 | Common:6; Rare:61 | ||||
chr11:506732-507001 | Common:3; Rare:92 | ||||
chr11:560720-561003 | Common:5; Rare:128 | ||||
chr11:576431-576531 | Rare:40 | ||||
chr11:615946-616187 | Common:1; Rare:78 | ||||
chr11:695724-695830 | Rare:35 | ||||
chr11:747249-747499 | Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777460-777607 | Common:1; Rare:65 | ||||
chr11:809503-809647 | Common:2; Rare:38 |