Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:6640646-6641132 | Common:7; Rare:156 | ||||
chr17:6651553-6651767 | Common:1; Rare:76 | ||||
chr17:7012297-7012731 | Rare:141 | ||||
chr17:7114606-7115177 | Common:10; Rare:109 | ||||
chr17:7179193-7179459 | Common:2; Rare:56 | ||||
chr17:7219806-7220196 | Common:5; Rare:166; Clinvar:9; Clinvar (benign):11; Clinvar (pathogenic):4 | ||||
chr17:7223970-7224247 | Rare:103; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):13 | ||||
chr17:7224318-7225060 | Common:5; Rare:270; Clinvar:23; Clinvar (benign):26; Clinvar (pathogenic):7 | ||||
chr17:7242246-7242660 | Common:1; Rare:120 | ||||
chr17:7251955-7252321 | Common:1; Rare:146 | ||||
chr17:7252465-7252723 | Common:2; Rare:100 | ||||
chr17:7260974-7261234 | Common:1; Rare:76 | ||||
chr17:7262458-7262685 | Common:2; Rare:53 | ||||
chr17:7307371-7307703 | Common:5; Rare:100 | ||||
chr17:7313383-7313621 | Common:1; Rare:97 |