Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:75878859-75879083 | Common:12; Rare:85 | ||||
chr7:75914944-75915176 | Common:2; Rare:78; Clinvar:2; Clinvar (benign):1 | ||||
chr7:75994510-75994772 | Common:4; Rare:132 | ||||
chr7:76047798-76048194 | Common:3; Rare:122 | ||||
chr7:76302861-76303009 | Rare:70; Clinvar:8; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
chr7:76303609-76303817 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr7:77537392-77537595 | Rare:69 | ||||
chr7:77696236-77696472 | Rare:95 | ||||
chr7:77798387-77798910 | Common:1; Rare:129 | ||||
chr7:79453559-79454134 | Common:3; Rare:141 | ||||
chr7:80134696-80134884 | Common:2; Rare:82 | ||||
chr7:80918939-80919348 | Common:3; Rare:134 | ||||
chr7:84194927-84195088 | Common:4; Rare:40 | ||||
chr7:87152334-87152493 | Common:2; Rare:56 | ||||
chr7:87345437-87345736 | Common:5; Rare:91 |