Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:184135344-184135398 | Rare:21 | ||||
chr3:184185880-184186204 | Common:4; Rare:117 | ||||
chr3:184248891-184249006 | Rare:61; Clinvar:5; Clinvar (benign):1 | ||||
chr3:184249450-184249777 | Common:1; Rare:97 | ||||
chr3:184314403-184314664 | Common:3; Rare:77 | ||||
chr3:185282838-185283006 | Common:1; Rare:45 | ||||
chr3:185498968-185499174 | Rare:73 | ||||
chr3:185586000-185586352 | Common:1; Rare:80 | ||||
chr3:186567291-186567615 | Common:3; Rare:85 | ||||
chr3:186806438-186806567 | Rare:42 | ||||
chr3:188153555-188153923 | Common:1; Rare:77 | ||||
chr3:188154060-188154215 | Rare:47 | ||||
chr3:190513823-190514107 | Common:2; Rare:82 | ||||
chr3:192917846-192918014 | Common:2; Rare:77 | ||||
chr3:195543241-195543475 | Common:3; Rare:91 |