Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:34997420-34997775 | Common:2; Rare:81; Clinvar (benign):1 | ||||
chr17:35242910-35243142 | Rare:81 | ||||
chr17:35373596-35373727 | Common:2; Rare:33 | ||||
chr17:35578492-35578702 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr17:35587212-35587525 | Rare:85 | ||||
chr17:35795621-35795760 | Rare:35 | ||||
chr17:35986593-35986863 | Common:1; Rare:69 | ||||
chr17:36486476-36486724 | Common:3; Rare:88 | ||||
chr17:36534803-36535054 | Common:3; Rare:107 | ||||
chr17:36544794-36544968 | Common:2; Rare:57 | ||||
chr17:36601491-36601616 | Rare:38 | ||||
chr17:37406792-37406924 | Rare:53 | ||||
chr17:37489709-37489941 | Common:1; Rare:92 | ||||
chr17:38428286-38428488 | Common:8; Rare:77 | ||||
chr17:38705018-38705334 | Common:2; Rare:74 |