Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:4303253-4303399 | Common:1; Rare:54 | ||||
chr3:4493165-4493503 | Rare:115; Clinvar:1; Clinvar (benign):1 | ||||
chr3:8501594-8501945 | Common:3; Rare:136 | ||||
chr3:9249617-9249750 | Common:1; Rare:35 | ||||
chr3:9362998-9363098 | Rare:35 | ||||
chr3:9792398-9792493 | Rare:28 | ||||
chr3:9792705-9793124 | Common:3; Rare:148 | ||||
chr3:9916960-9917154 | Common:2; Rare:42 | ||||
chr3:9933563-9933877 | Common:1; Rare:121; Clinvar:2 | ||||
chr3:10026329-10026465 | Rare:40 | ||||
chr3:10115520-10115702 | Common:3; Rare:65 | ||||
chr3:11154342-11154542 | Common:4; Rare:52 | ||||
chr3:11719453-11719579 | Rare:37 | ||||
chr3:12664101-12664300 | Common:1; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
chr3:13480040-13480324 | Common:2; Rare:67 |