Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111140028-111140306 | Common:2; Rare:96 | ||||
chr1:111473847-111474003 | Common:1; Rare:27 | ||||
chr1:111619548-111619847 | Common:2; Rare:100 | ||||
chr1:112396022-112396272 | Common:1; Rare:77 | ||||
chr1:112619099-112619199 | Rare:36 | ||||
chr1:112619685-112619868 | Common:1; Rare:68 | ||||
chr1:112956188-112956504 | Common:5; Rare:135; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073085-113073221 | Common:1; Rare:46 | ||||
chr1:113390391-113390512 | Common:1; Rare:35 | ||||
chr1:113904793-113905385 | Common:7; Rare:173; Clinvar (benign):1 | ||||
chr1:114581587-114581868 | Rare:114 | ||||
chr1:115338224-115338504 | Common:1; Rare:67 | ||||
chr1:116398753-116399084 | Common:1; Rare:69 | ||||
chr1:116400752-116400917 | Common:1; Rare:38; Clinvar (pathogenic):1 | ||||
chr1:117060174-117060349 | Common:2; Rare:42 |