Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:66115261-66115353 | Rare:21 | ||||
chr7:66681987-66682207 | Common:6; Rare:100 | ||||
chr7:73683419-73683617 | Common:2; Rare:78 | ||||
chr7:73738798-73739024 | Common:1; Rare:64 | ||||
chr7:74254385-74254541 | Rare:74 | ||||
chr7:75878833-75879088 | Common:12; Rare:92 | ||||
chr7:75914944-75915160 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr7:75994522-75994772 | Common:4; Rare:129 | ||||
chr7:76047980-76048180 | Common:1; Rare:62 | ||||
chr7:76302862-76303075 | Rare:89; Clinvar:9; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr7:76303781-76303817 | Rare:20; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr7:77696242-77696483 | Rare:100 | ||||
chr7:77697026-77697159 | Common:1; Rare:46 | ||||
chr7:77798353-77798971 | Common:1; Rare:146 | ||||
chr7:79453589-79453640 | Rare:19 |