Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:123008785-123009023 | Common:5; Rare:65; Clinvar:4; Clinvar (benign):5 | ||||
chr10:124093539-124093812 | Common:2; Rare:51 | ||||
chr10:124791756-124791944 | Common:1; Rare:98 | ||||
chr10:124801730-124801846 | Rare:38 | ||||
chr10:125719480-125719755 | Common:1; Rare:100 | ||||
chr10:125823207-125823639 | Common:1; Rare:154; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905297-126905474 | Rare:69 | ||||
chr10:128047450-128047635 | Common:2; Rare:60 | ||||
chr10:132331872-132332155 | Common:12; Rare:69 | ||||
chr10:133308835-133308974 | Rare:66 | ||||
chr11:207355-207719 | Common:8; Rare:119 | ||||
chr11:208638-208855 | Rare:81 | ||||
chr11:236335-236503 | Common:6; Rare:49 | ||||
chr11:236848-237071 | Common:2; Rare:85 | ||||
chr11:307579-308437 | Common:33; Rare:231 |