Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6637274-6637517 | Rare:69 | ||||
chr1:7819166-7819418 | Common:2; Rare:63 | ||||
chr1:8010622-8010683 | Rare:7 | ||||
chr1:8025123-8025277 | Common:1; Rare:31 | ||||
chr1:8121353-8121608 | Common:3; Rare:45 | ||||
chr1:8373661-8373797 | Common:1; Rare:36 | ||||
chr1:9181836-9182026 | Rare:37 | ||||
chr1:9182263-9182350 | Rare:22 | ||||
chr1:9182368-9182471 | Common:2; Rare:25 | ||||
chr1:9242654-9242867 | Common:1; Rare:52 | ||||
chr1:9244770-9244961 | Common:2; Rare:47; Clinvar (benign):1 | ||||
chr1:9305568-9305752 | Common:1; Rare:34 | ||||
chr1:9687493-9687633 | Common:1; Rare:36 | ||||
chr1:10641733-10641903 | Common:2; Rare:32 | ||||
chr1:10683320-10683512 | Common:1; Rare:42 |