Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:44573896-44574053 | Common:3; Rare:42 | ||||
chr7:45111675-45111799 | Common:1; Rare:46 | ||||
chr7:48089004-48089278 | Common:4; Rare:67 | ||||
chr7:56051424-56051840 | Common:1; Rare:159; Clinvar:5; Clinvar (benign):1 | ||||
chr7:66114773-66114895 | Common:1; Rare:62 | ||||
chr7:66682009-66682184 | Common:5; Rare:85 | ||||
chr7:73683441-73683622 | Common:3; Rare:73 | ||||
chr7:74254385-74254528 | Rare:66 | ||||
chr7:75914940-75915158 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
chr7:76047950-76048180 | Common:1; Rare:78 | ||||
chr7:76302893-76302996 | Rare:42; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr7:77696253-77696460 | Rare:80 | ||||
chr7:79453610-79453639 | Rare:10 | ||||
chr7:79453950-79454024 | Common:1; Rare:18 | ||||
chr7:80134511-80134897 | Common:4; Rare:133 |