Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:129488507-129488738 | Common:2; Rare:65 | ||||
chr9:136438935-136439099 | Rare:63; Clinvar (pathogenic):1 | ||||
chr9:136728148-136728278 | Common:3; Rare:59 | ||||
chr9:137267011-137267256 | Common:6; Rare:88 | ||||
chrM:260-818 | |||||
chrM:972-1017 | |||||
chrM:1375-1764 | |||||
chrM:1805-1925 | |||||
chrM:1959-2295 | |||||
chrM:6523-6636 | |||||
chrM:6643-6687 | |||||
chrM:6891-6976 | |||||
chrM:15383-15895 | |||||
chrM:16319-16410 | |||||
chrX:15675381-15675478 | Common:4; Rare:15 |