Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:41092490-41092652 | Rare:78 | ||||
chr22:41413887-41414063 | Common:1; Rare:52 | ||||
chr22:41518412-41518561 | Common:2; Rare:37; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr22:42369237-42369498 | Common:4; Rare:62 | ||||
chr22:42995173-42995262 | Rare:12 | ||||
chr22:46069936-46070072 | Rare:37 | ||||
chr22:46080057-46080336 | Common:1; Rare:91 | ||||
chr3:536027-536273 | Common:3; Rare:98 | ||||
chr3:4831347-4831443 | Rare:19 | ||||
chr3:9791402-9791725 | Rare:77 | ||||
chr3:13629068-13629220 | Rare:59 | ||||
chr3:14125743-14125912 | Common:1; Rare:44 | ||||
chr3:15738352-15738530 | Common:2; Rare:41 | ||||
chr3:30644545-30644856 | Rare:74; Clinvar:3; Clinvar (benign):5 | ||||
chr3:39384274-39384474 | Common:4; Rare:46 |