Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:157110650-157110926 | Common:2; Rare:66 | ||||
chr3:157174855-157175263 | Common:3; Rare:179 | ||||
chr3:159732274-159732396 | Common:1; Rare:20 | ||||
chr3:168026825-168026877 | Rare:11 | ||||
chr3:168249479-168249822 | Common:3; Rare:83 | ||||
chr3:168249972-168250194 | Rare:60 | ||||
chr3:169765022-169765174 | Rare:70; Clinvar:5; Clinvar (pathogenic):3 | ||||
chr3:183447427-183447712 | Common:2; Rare:71 | ||||
chr3:184015628-184015835 | Rare:27 | ||||
chr3:184710627-184710867 | Rare:41 | ||||
chr3:184710872-184710892 | Rare:4 | ||||
chr3:184710913-184711093 | Common:1; Rare:66 | ||||
chr3:188270432-188270544 | Common:1; Rare:18 | ||||
chr3:194205788-194205897 | Rare:21 | ||||
chr3:194476929-194477149 | Rare:41 |