Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:112619099-112619236 | Rare:49 | ||||
chr1:112619642-112619877 | Common:2; Rare:84 | ||||
chr1:112956104-112956393 | Common:4; Rare:110; Clinvar:10; Clinvar (benign):3 | ||||
chr1:113073095-113073245 | Common:1; Rare:56 | ||||
chr1:113390209-113390497 | Common:1; Rare:72 | ||||
chr1:113812269-113812579 | Common:2; Rare:123 | ||||
chr1:113904824-113905387 | Common:7; Rare:169; Clinvar (benign):1 | ||||
chr1:116123937-116124156 | Common:2; Rare:62 | ||||
chr1:116570975-116571197 | Common:2; Rare:64 | ||||
chr1:117060220-117060332 | Common:1; Rare:26 | ||||
chr1:117367685-117367951 | Rare:52 | ||||
chr1:117368205-117368479 | Rare:70 | ||||
chr1:117929560-117929806 | Common:4; Rare:72 | ||||
chr1:118914355-118914636 | Common:1; Rare:63 | ||||
chr1:119140634-119140785 | Common:1; Rare:49 |