Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114780548-114780857 | Common:2; Rare:112 | ||||
chr1:115641662-115641853 | Common:2; Rare:41 | ||||
chr1:115641926-115642197 | Common:3; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
chr1:115642651-115643054 | Common:7; Rare:83 | ||||
chr1:115976156-115976378 | Common:1; Rare:42 | ||||
chr1:116111342-116111475 | Rare:26 | ||||
chr1:116373067-116373422 | Rare:113 | ||||
chr1:116374037-116374221 | Rare:59 | ||||
chr1:116544917-116545113 | Common:3; Rare:32 | ||||
chr1:116570324-116570607 | Common:1; Rare:63 | ||||
chr1:116570857-116571221 | Common:5; Rare:102 | ||||
chr1:117001352-117001444 | Common:1; Rare:25 | ||||
chr1:117001506-117001796 | Common:2; Rare:43 | ||||
chr1:117059679-117060391 | Common:12; Rare:187 | ||||
chr1:117060716-117060859 | Rare:38 |