Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:110339148-110339482 | Common:2; Rare:103 | ||||
chr1:110407616-110407809 | Common:2; Rare:88 | ||||
chr1:111139230-111139512 | Common:2; Rare:55 | ||||
chr1:111140069-111140305 | Common:2; Rare:80 | ||||
chr1:111199844-111200012 | Rare:31 | ||||
chr1:111200588-111200715 | Common:1; Rare:30 | ||||
chr1:111739339-111739560 | Common:2; Rare:57 | ||||
chr1:112396062-112396272 | Common:1; Rare:67 | ||||
chr1:112466163-112466351 | Common:3; Rare:44 | ||||
chr1:112619091-112619236 | Rare:54 | ||||
chr1:112619643-112619877 | Common:2; Rare:83 | ||||
chr1:112956178-112956437 | Common:4; Rare:116; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073105-113073261 | Common:1; Rare:69 | ||||
chr1:113390215-113390497 | Common:1; Rare:70 | ||||
chr1:113905026-113905380 | Common:4; Rare:99 |