Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:15699452-15699797 | Common:4; Rare:96 | ||||
chr17:15999566-16000200 | Common:4; Rare:260; Clinvar:6; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
chr17:16215477-16215615 | Common:1; Rare:66 | ||||
chr17:16217105-16217247 | Rare:45; Clinvar:1 | ||||
chr17:16653795-16653916 | Rare:41 | ||||
chr17:17042094-17042114 | Rare:3 | ||||
chr17:17237101-17237191 | Common:1; Rare:40; Clinvar:1; Clinvar (benign):3 | ||||
chr17:17237389-17237704 | Common:4; Rare:71 | ||||
chr17:17280670-17280911 | Common:3; Rare:100 | ||||
chr17:17281151-17281405 | Rare:95 | ||||
chr17:17476848-17477073 | Common:3; Rare:66 | ||||
chr17:17496355-17496513 | Rare:43 | ||||
chr17:17591380-17591485 | Rare:35 | ||||
chr17:17591577-17591932 | Common:2; Rare:103 | ||||
chr17:17682800-17682952 | Common:3; Rare:40 |