Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75904879-75904971 | Common:1; Rare:32 | ||||
chr17:75979126-75979272 | Rare:38; Clinvar:4 | ||||
chr17:76103703-76103867 | Common:4; Rare:57 | ||||
chr17:76726487-76726865 | Common:5; Rare:132 | ||||
chr17:76737316-76737599 | Common:3; Rare:105 | ||||
chr17:77280413-77280615 | Common:1; Rare:33 | ||||
chr17:78168457-78168617 | Rare:44 | ||||
chr17:78187045-78187365 | Common:3; Rare:101 | ||||
chr17:78840745-78841114 | Common:2; Rare:139 | ||||
chr17:79009696-79009924 | Common:9; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
chr17:80220318-80220431 | Rare:44; Clinvar:1 | ||||
chr17:80415126-80415197 | Common:1; Rare:50 | ||||
chr17:80415387-80415492 | Common:4; Rare:40 | ||||
chr17:81395179-81395463 | Common:1; Rare:72 | ||||
chr17:81636916-81637211 | Common:2; Rare:119 |