Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:130136310-130136457 | Common:6; Rare:63 | ||||
chr10:132331784-132332182 | Common:17; Rare:130 | ||||
chr10:133308844-133308988 | Rare:65 | ||||
chr10:133393993-133394267 | Common:2; Rare:126 | ||||
chr11:207381-207726 | Common:7; Rare:100 | ||||
chr11:208673-208842 | Rare:65 | ||||
chr11:236340-236541 | Common:7; Rare:62 | ||||
chr11:236917-237044 | Common:1; Rare:50 | ||||
chr11:313877-314173 | Rare:61 | ||||
chr11:506749-506981 | Common:2; Rare:77 | ||||
chr11:560694-561008 | Common:6; Rare:149 | ||||
chr11:576431-576519 | Rare:35 | ||||
chr11:615946-616103 | Common:1; Rare:47 | ||||
chr11:695766-695830 | Rare:27 | ||||
chr11:747284-747493 | Rare:89; Clinvar:2; Clinvar (benign):1 |