Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117060685-117060842 | Rare:39 | ||||
chr1:117121664-117122009 | Common:1; Rare:112 | ||||
chr1:117367218-117367538 | Common:7; Rare:107 | ||||
chr1:117605802-117606088 | Rare:91 | ||||
chr1:117929488-117929848 | Common:4; Rare:102 | ||||
chr1:118914444-118914647 | Common:2; Rare:39 | ||||
chr1:119140274-119140547 | Common:2; Rare:79 | ||||
chr1:119140563-119140865 | Common:1; Rare:100; Clinvar (pathogenic):1 | ||||
chr1:119141086-119141157 | Rare:14 | ||||
chr1:119647665-119647899 | Rare:36 | ||||
chr1:119711738-119711997 | Common:2; Rare:72; Clinvar:4; Clinvar (benign):2 | ||||
chr1:120176239-120176292 | Rare:8 | ||||
chr1:120176332-120176656 | Common:1; Rare:60 | ||||
chr1:145214494-145214701 | Rare:18 | ||||
chr1:145608273-145608306 | Common:1; Rare:13 |