Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:184298966-184299269 | Common:2; Rare:90 | ||||
chr3:184314421-184314664 | Common:3; Rare:72 | ||||
chr3:184335815-184335937 | Common:1; Rare:36 | ||||
chr3:184361601-184361921 | Rare:72 | ||||
chr3:184711926-184712272 | Common:2; Rare:113 | ||||
chr3:185282855-185283026 | Common:1; Rare:42 | ||||
chr3:185498911-185499140 | Rare:84 | ||||
chr3:185824956-185825150 | Rare:60 | ||||
chr3:186567291-186567469 | Common:3; Rare:42 | ||||
chr3:186806438-186806567 | Rare:42 | ||||
chr3:188153835-188153977 | Common:1; Rare:28 | ||||
chr3:188154067-188154227 | Rare:52 | ||||
chr3:188947534-188947663 | Rare:24 | ||||
chr3:190120388-190120662 | Rare:117; Clinvar (pathogenic):1 | ||||
chr3:193241074-193241368 | Common:2; Rare:96 |