Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:57555979-57556322 | Rare:86 | ||||
chr3:57597290-57597851 | Common:7; Rare:169 | ||||
chr3:58332822-58332973 | Common:3; Rare:46 | ||||
chr3:58433794-58433938 | Rare:58; Clinvar:2; Clinvar (benign):3 | ||||
chr3:58537152-58537280 | Common:1; Rare:27 | ||||
chr3:61251399-61251593 | Common:4; Rare:51 | ||||
chr3:61561412-61561657 | Common:2; Rare:87 | ||||
chr3:62318932-62319088 | Rare:63 | ||||
chr3:63863743-63864158 | Common:8; Rare:138 | ||||
chr3:63864437-63864539 | Common:2; Rare:35 | ||||
chr3:66998024-66998330 | Rare:74 | ||||
chr3:67654583-67654727 | Common:1; Rare:51 | ||||
chr3:69013214-69013359 | Rare:42 | ||||
chr3:69013590-69013838 | Common:1; Rare:78 | ||||
chr3:69084786-69085079 | Common:3; Rare:78 |