Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:124748753-124748997 | Common:2; Rare:54 | ||||
chr5:126423324-126423498 | Rare:43 | ||||
chr5:127030526-127030736 | Common:2; Rare:47 | ||||
chr5:127290666-127290839 | Rare:36 | ||||
chr5:129094471-129094759 | Common:3; Rare:115 | ||||
chr5:129460106-129460314 | Common:4; Rare:32 | ||||
chr5:131170693-131171002 | Common:1; Rare:63; Clinvar (benign):1 | ||||
chr5:131635163-131635424 | Common:1; Rare:98 | ||||
chr5:131796936-131797208 | Rare:79 | ||||
chr5:132369602-132369752 | Common:3; Rare:44 | ||||
chr5:132369883-132369914 | Common:2; Rare:8; Clinvar (benign):2 | ||||
chr5:132866471-132866699 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
chr5:133051862-133052114 | Rare:94 | ||||
chr5:133968576-133968718 | Rare:56 | ||||
chr5:134004647-134004855 | Common:1; Rare:77 |