Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:51260879-51260947 | Common:2; Rare:31 | ||||
chr17:54968599-54968793 | Common:3; Rare:92 | ||||
chr17:56914005-56914186 | Common:1; Rare:48 | ||||
chr17:57084971-57085335 | Rare:124 | ||||
chr17:57850002-57850274 | Common:1; Rare:89 | ||||
chr17:58007151-58007390 | Common:1; Rare:116 | ||||
chr17:58219223-58219284 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):3 | ||||
chr17:58352125-58352436 | Common:5; Rare:131 | ||||
chr17:58692559-58692628 | Common:1; Rare:38; Clinvar (benign):12 | ||||
chr17:59106707-59106970 | Common:2; Rare:86; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155156-59155502 | Common:2; Rare:76 | ||||
chr17:59331486-59331778 | Common:2; Rare:94 | ||||
chr17:59619563-59620064 | Common:3; Rare:176 | ||||
chr17:59707397-59707727 | Common:3; Rare:90; Clinvar (benign):3 | ||||
chr17:59892739-59893161 | Common:1; Rare:115 |