Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:115642443-115642553 | Common:1; Rare:23 | ||||
chr1:116373077-116373439 | Common:1; Rare:120 | ||||
chr1:116399169-116399543 | Rare:64 | ||||
chr1:116570971-116571156 | Common:2; Rare:54 | ||||
chr1:116646949-116646985 | Rare:9 | ||||
chr1:116667672-116667845 | Common:1; Rare:65 | ||||
chr1:116909580-116909880 | Common:3; Rare:76 | ||||
chr1:117060065-117060374 | Common:6; Rare:87 | ||||
chr1:117121695-117121962 | Common:1; Rare:81 | ||||
chr1:117367492-117367723 | Common:1; Rare:55 | ||||
chr1:117605768-117606080 | Rare:95 | ||||
chr1:117929532-117929863 | Common:4; Rare:99 | ||||
chr1:118185153-118185413 | Common:1; Rare:64 | ||||
chr1:119140584-119140796 | Common:1; Rare:80; Clinvar (pathogenic):1 | ||||
chr1:119648096-119648367 | Common:3; Rare:91 |