Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:39383582-39383651 | Rare:16 | ||||
chr3:40309477-40309847 | Common:9; Rare:125 | ||||
chr3:40524845-40525013 | Rare:47 | ||||
chr3:42581848-42582071 | Common:3; Rare:78 | ||||
chr3:42600522-42600728 | Common:1; Rare:82 | ||||
chr3:42804312-42804620 | Common:2; Rare:80 | ||||
chr3:43690793-43691033 | Common:5; Rare:131; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr3:44477622-44477695 | Rare:21 | ||||
chr3:44624915-44625088 | Common:2; Rare:51 | ||||
chr3:44761590-44761835 | Common:3; Rare:88 | ||||
chr3:44861767-44861919 | Common:2; Rare:68 | ||||
chr3:44976113-44976283 | Common:2; Rare:71 | ||||
chr3:45689177-45689463 | Common:1; Rare:96 | ||||
chr3:47380828-47381064 | Rare:68 | ||||
chr3:47381448-47381590 | Rare:32 |