Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:55491719-55491836 | Rare:29; Clinvar (pathogenic):1 | ||||
chr16:56617400-56617542 | Common:1; Rare:29 | ||||
chr16:66695869-66696058 | Rare:34 | ||||
chr16:72100263-72100555 | Common:3; Rare:74 | ||||
chr16:72665002-72665145 | Rare:37 | ||||
chr16:74368122-74368376 | Common:1; Rare:71 | ||||
chr16:85370912-85371170 | Rare:72 | ||||
chr16:88721405-88721646 | Common:1; Rare:117; Clinvar:1 | ||||
chr16:90047766-90048079 | Common:9; Rare:33 | ||||
chr17:909606-909897 | Common:4; Rare:69 | ||||
chr17:2374986-2375264 | Common:3; Rare:54 | ||||
chr17:2375295-2375385 | Common:2; Rare:21 | ||||
chr17:4858937-4859124 | Common:1; Rare:46 | ||||
chr17:7310778-7311116 | Rare:84 | ||||
chr17:7887415-7887824 | Common:1; Rare:82 |