Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113758808-113758948 | Common:1; Rare:34 | ||||
chr1:113759466-113759610 | Common:1; Rare:47 | ||||
chr1:113759644-113759912 | Rare:51 | ||||
chr1:113812239-113812560 | Common:2; Rare:135 | ||||
chr1:113904785-113905333 | Common:5; Rare:155; Clinvar (benign):1 | ||||
chr1:113929442-113929671 | Common:1; Rare:74 | ||||
chr1:114581580-114581814 | Common:1; Rare:106 | ||||
chr1:114716713-114717005 | Common:4; Rare:110; Clinvar:5; Clinvar (benign):1 | ||||
chr1:115089455-115089556 | Rare:40 | ||||
chr1:117060243-117060341 | Common:2; Rare:26 | ||||
chr1:117367297-117367494 | Common:4; Rare:74 | ||||
chr1:117929615-117929815 | Common:3; Rare:53 | ||||
chr1:119140627-119140735 | Rare:32 | ||||
chr1:120176343-120176413 | Rare:12 | ||||
chr1:145823911-145824248 | Rare:118 |