Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:52664285-52664431 | Common:2; Rare:47 | ||||
chr6:53359357-53359578 | Common:4; Rare:64 | ||||
chr6:53793667-53793794 | Common:2; Rare:20 | ||||
chr6:56540612-56540826 | Rare:33 | ||||
chr6:57257983-57258119 | Rare:25 | ||||
chr6:57961320-57961531 | Rare:80 | ||||
chr6:71420827-71421018 | Common:1; Rare:59 | ||||
chr6:73517709-73518286 | Common:3; Rare:155 | ||||
chr6:75087729-75088009 | Common:1; Rare:39 | ||||
chr6:75143256-75143489 | Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
chr6:75165643-75165882 | Common:3; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
chr6:79025563-79025830 | Rare:48; Clinvar (pathogenic):1 | ||||
chr6:81753341-81753509 | Rare:55 | ||||
chr6:85678676-85678922 | Rare:97 | ||||
chr6:85865702-85865874 | Common:1; Rare:47 |