Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7548376-7548553 | Common:2; Rare:21 | ||||
chr17:7548816-7549045 | Rare:60 | ||||
chr17:7558045-7558340 | Common:2; Rare:62 | ||||
chr17:7558362-7558813 | Rare:88 | ||||
chr17:7561101-7561396 | Rare:51 | ||||
chr17:7561695-7561925 | Rare:67 | ||||
chr17:7572367-7572920 | Common:1; Rare:236 | ||||
chr17:7573217-7573286 | Common:3; Rare:25 | ||||
chr17:7573654-7573884 | Common:1; Rare:85 | ||||
chr17:7574664-7574714 | Rare:20 | ||||
chr17:7579499-7579677 | Rare:50 | ||||
chr17:7583590-7583951 | Common:1; Rare:145; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr17:7584005-7584172 | Rare:49 | ||||
chr17:7614244-7614495 | Common:1; Rare:51 | ||||
chr17:7614567-7614689 | Rare:28 |