Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:110034439-110034626 | Rare:51 | ||||
chr1:110339113-110339480 | Common:1; Rare:111 | ||||
chr1:110407368-110407428 | Rare:20 | ||||
chr1:110407596-110407853 | Common:4; Rare:107 | ||||
chr1:110963827-110964226 | Rare:134 | ||||
chr1:111139792-111139881 | Rare:13 | ||||
chr1:111140049-111140296 | Common:2; Rare:83 | ||||
chr1:111619659-111619847 | Common:2; Rare:74 | ||||
chr1:111739358-111739699 | Common:3; Rare:95 | ||||
chr1:112396009-112396262 | Common:1; Rare:78 | ||||
chr1:112619090-112619199 | Rare:42 | ||||
chr1:112619642-112619880 | Common:2; Rare:86 | ||||
chr1:112674597-112674898 | Common:1; Rare:64 | ||||
chr1:112956175-112956659 | Common:6; Rare:160; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073081-113073238 | Common:1; Rare:56 |