Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:152268838-152268958 | Rare:44 | ||||
chr3:155854380-155854756 | Rare:103 | ||||
chr3:156674378-156674629 | Common:3; Rare:71 | ||||
chr3:157160134-157160288 | Rare:65 | ||||
chr3:158105739-158105878 | Common:5; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
chr3:158801997-158802158 | Common:2; Rare:75 | ||||
chr3:160399530-160399669 | Rare:28 | ||||
chr3:179604620-179604838 | Common:1; Rare:76 | ||||
chr3:183099469-183099742 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):3 | ||||
chr3:184135221-184135391 | Common:2; Rare:51; Clinvar:5 | ||||
chr3:184249515-184249771 | Common:1; Rare:81 | ||||
chr3:185282838-185283001 | Common:1; Rare:43 | ||||
chr3:185498974-185499149 | Rare:61 | ||||
chr3:193593117-193593292 | Rare:56; Clinvar:1 | ||||
chr3:195543251-195543483 | Common:3; Rare:95 |