Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:179604614-179604852 | Common:2; Rare:87 | ||||
chr3:180602020-180602258 | Common:1; Rare:81 | ||||
chr3:180989629-180989823 | Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
chr3:183697729-183697909 | Rare:87 | ||||
chr3:184135221-184135391 | Common:2; Rare:51; Clinvar:5 | ||||
chr3:184248869-184249021 | Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
chr3:184249550-184249776 | Common:1; Rare:79 | ||||
chr3:184298944-184299272 | Common:3; Rare:101 | ||||
chr3:184361590-184361770 | Rare:48 | ||||
chr3:184711953-184712272 | Common:1; Rare:103 | ||||
chr3:185282855-185283019 | Common:1; Rare:40 | ||||
chr3:185498919-185499140 | Rare:81 | ||||
chr3:186567286-186567431 | Common:3; Rare:39 | ||||
chr3:186783252-186783628 | Common:1; Rare:158 | ||||
chr3:186784131-186784212 | Rare:30 |