Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:43994773-43994984 | Rare:48 | ||||
chr3:44685615-44685725 | Common:1; Rare:34 | ||||
chr3:45224797-45224866 | Common:1; Rare:10 | ||||
chr3:47164784-47164947 | Common:2; Rare:35 | ||||
chr3:47888225-47888278 | Common:1; Rare:15 | ||||
chr3:50376163-50376435 | Rare:68 | ||||
chr3:52298853-52298907 | Rare:8 | ||||
chr3:52407280-52407432 | Rare:43; Clinvar:2; Clinvar (benign):6 | ||||
chr3:54124032-54124306 | Rare:48 | ||||
chr3:54125487-54125616 | Rare:17 | ||||
chr3:57583896-57584226 | Common:1; Rare:63 | ||||
chr3:61560553-61560823 | Common:1; Rare:85 | ||||
chr3:64720506-64720709 | Rare:43 | ||||
chr3:65597088-65597171 | Rare:15 | ||||
chr3:66195525-66195649 | Common:2; Rare:34 |