Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112395970-112396257 | Common:2; Rare:90 | ||||
chr1:112619112-112619236 | Rare:43 | ||||
chr1:112619642-112619880 | Common:2; Rare:86 | ||||
chr1:112674597-112674758 | Common:1; Rare:32 | ||||
chr1:112956180-112956467 | Common:5; Rare:126; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073105-113073221 | Common:1; Rare:43 | ||||
chr1:113904831-113905392 | Common:7; Rare:167; Clinvar (benign):1 | ||||
chr1:114581578-114581832 | Common:1; Rare:113 | ||||
chr1:115089435-115089612 | Common:2; Rare:71 | ||||
chr1:116570968-116571197 | Common:2; Rare:66 | ||||
chr1:117121726-117121935 | Common:1; Rare:56 | ||||
chr1:117367653-117367723 | Rare:13 | ||||
chr1:117605783-117606053 | Rare:78 | ||||
chr1:117929560-117929811 | Common:4; Rare:75 | ||||
chr1:119140634-119140785 | Common:1; Rare:49 |