Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:101680905-101681158 | Common:2; Rare:52 | ||||
chr3:107240630-107240747 | Rare:49 | ||||
chr3:112770121-112770355 | Rare:56 | ||||
chr3:120095094-120095249 | Rare:48 | ||||
chr3:122437261-122437539 | Common:1; Rare:53 | ||||
chr3:123664199-123664462 | Rare:59; Clinvar:4; Clinvar (benign):5 | ||||
chr3:124816174-124816535 | Common:3; Rare:56 | ||||
chr3:125916322-125916621 | Common:4; Rare:89 | ||||
chr3:129794435-129794578 | Rare:17 | ||||
chr3:130111470-130111785 | Common:3; Rare:77 | ||||
chr3:131361637-131361916 | Common:3; Rare:82 | ||||
chr3:133491075-133491394 | Rare:65 | ||||
chr3:133756695-133756947 | Common:4; Rare:73; Clinvar (benign):2 | ||||
chr3:133757528-133757607 | Common:2; Rare:21 | ||||
chr3:133945232-133945319 | Rare:31 |