Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:127030539-127030768 | Common:2; Rare:53 | ||||
chr5:131170662-131171002 | Common:1; Rare:78; Clinvar (benign):1 | ||||
chr5:131796975-131797215 | Rare:64 | ||||
chr5:132490774-132491021 | Rare:64 | ||||
chr5:132556895-132557018 | Rare:50; Clinvar:1 | ||||
chr5:132963292-132963788 | Common:3; Rare:124 | ||||
chr5:133051862-133052161 | Rare:104 | ||||
chr5:133968573-133968737 | Rare:64 | ||||
chr5:134004649-134004855 | Common:1; Rare:76 | ||||
chr5:134004933-134005019 | Rare:19 | ||||
chr5:134632733-134632918 | Rare:37 | ||||
chr5:134648689-134648816 | Rare:37 | ||||
chr5:134845845-134846089 | Rare:111 | ||||
chr5:134874261-134874430 | Common:1; Rare:88 | ||||
chr5:136028937-136029068 | Rare:44; Clinvar:1 |