Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44324782-44324963 | Common:2; Rare:62 | ||||
chr17:44503383-44503540 | Rare:66 | ||||
chr17:44899386-44899480 | Rare:40 | ||||
chr17:45060971-45061345 | Common:2; Rare:102 | ||||
chr17:46923077-46923195 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):7 | ||||
chr17:47649510-47650002 | Common:1; Rare:175 | ||||
chr17:47831462-47831689 | Rare:75 | ||||
chr17:48048051-48048379 | Rare:89 | ||||
chr17:48048593-48048834 | Common:4; Rare:41 | ||||
chr17:49210210-49210712 | Common:3; Rare:84 | ||||
chr17:49788570-49788691 | Rare:33 | ||||
chr17:50373149-50373229 | Common:2; Rare:41 | ||||
chr17:50719467-50719830 | Rare:118 | ||||
chr17:50866352-50866611 | Common:3; Rare:78 | ||||
chr17:51260376-51260575 | Common:3; Rare:93 |