Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:77127702-77127880 | Rare:32 | ||||
chr17:77129954-77130110 | Rare:26 | ||||
chr17:77140654-77141054 | Common:2; Rare:139 | ||||
chr17:77141418-77141470 | Rare:16 | ||||
chr17:77319471-77319619 | Common:3; Rare:42; Clinvar:1; Clinvar (benign):3 | ||||
chr17:77319809-77319926 | Rare:23 | ||||
chr17:77374467-77374653 | Rare:37 | ||||
chr17:77450280-77450567 | Common:2; Rare:61 | ||||
chr17:77453915-77454102 | Common:2; Rare:43 | ||||
chr17:78128624-78128868 | Common:7; Rare:62 | ||||
chr17:78130635-78130833 | Rare:36 | ||||
chr17:78187029-78187423 | Common:3; Rare:141 | ||||
chr17:78782206-78782572 | Common:9; Rare:122 | ||||
chr17:78840740-78841114 | Common:2; Rare:141 | ||||
chr17:79009696-79009924 | Common:9; Rare:67; Clinvar:2; Clinvar (benign):1 |