Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:166342519-166342653 | Common:3; Rare:51 | ||||
chr6:166956539-166956687 | Common:2; Rare:51; Clinvar:3 | ||||
chr6:166999074-166999424 | Common:1; Rare:118 | ||||
chr6:167826810-167827213 | Common:2; Rare:199 | ||||
chr6:167966533-167966793 | Common:2; Rare:52 | ||||
chr6:169701975-169702339 | Common:5; Rare:159 | ||||
chr6:169751520-169751644 | Rare:45; Clinvar (benign):1 | ||||
chr6:170306559-170306799 | Common:1; Rare:79 | ||||
chr6:170554210-170554404 | Common:1; Rare:63 | ||||
chr7:519089-519294 | Rare:52 | ||||
chr7:727261-727317 | Rare:16; Clinvar:1 | ||||
chr7:975493-975674 | Common:1; Rare:82 | ||||
chr7:1028301-1028466 | Rare:63 | ||||
chr7:1055180-1055390 | Common:1; Rare:75 | ||||
chr7:1537324-1537490 | Rare:55 |