Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:65982188-65982328 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):3 | ||||
chr7:66114773-66114898 | Common:1; Rare:62 | ||||
chr7:66115194-66115353 | Rare:35 | ||||
chr7:66205144-66205344 | Rare:43 | ||||
chr7:66682015-66682147 | Common:4; Rare:62 | ||||
chr7:66996524-66996850 | Common:3; Rare:73 | ||||
chr7:73683419-73683628 | Common:3; Rare:86 | ||||
chr7:73738786-73739006 | Common:1; Rare:63 | ||||
chr7:73842510-73842682 | Common:5; Rare:22 | ||||
chr7:74254352-74254528 | Rare:82 | ||||
chr7:75878859-75879094 | Common:12; Rare:89 | ||||
chr7:75994590-75994779 | Common:3; Rare:101 | ||||
chr7:76047950-76048188 | Common:2; Rare:81 | ||||
chr7:76302862-76303073 | Rare:89; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr7:77696236-77696465 | Rare:91 |