Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111204357-111204639 | Rare:70 | ||||
chr1:111346526-111346655 | Common:1; Rare:37 | ||||
chr1:111619482-111619847 | Common:2; Rare:111 | ||||
chr1:111739361-111739661 | Common:3; Rare:84 | ||||
chr1:112619102-112619236 | Rare:48 | ||||
chr1:112619682-112619875 | Common:2; Rare:72 | ||||
chr1:112956173-112956467 | Common:5; Rare:126; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073085-113073238 | Common:1; Rare:55 | ||||
chr1:113812264-113812579 | Common:2; Rare:124 | ||||
chr1:113905026-113905399 | Common:5; Rare:103 | ||||
chr1:114669999-114670209 | Common:1; Rare:65 | ||||
chr1:114780549-114780723 | Rare:70 | ||||
chr1:114854742-114854863 | Common:1; Rare:31 | ||||
chr1:115641811-115642007 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
chr1:116373083-116373435 | Common:1; Rare:117 |