Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:11975323-11975694 | Common:3; Rare:68 | ||||
chr17:16026361-16026663 | Rare:76; Clinvar (benign):2 | ||||
chr17:16061850-16062030 | Common:1; Rare:51 | ||||
chr17:16382660-16382869 | Rare:62 | ||||
chr17:16438666-16439018 | Rare:83 | ||||
chr17:16822543-16822839 | Common:5; Rare:28 | ||||
chr17:16831247-16831470 | Common:1; Rare:56 | ||||
chr17:17739062-17739123 | Rare:11 | ||||
chr17:17739126-17739206 | Rare:13 | ||||
chr17:17836186-17836437 | Common:3; Rare:68 | ||||
chr17:18449884-18450187 | Common:2; Rare:36 | ||||
chr17:18572608-18572724 | Common:1; Rare:26 | ||||
chr17:19738169-19738454 | Common:1; Rare:110 | ||||
chr17:28525063-28525388 | Common:2; Rare:57 | ||||
chr17:28880456-28880746 | Common:2; Rare:91 |