Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114757947-114758112 | Common:3; Rare:49 | ||||
chr1:114780549-114780787 | Common:1; Rare:91 | ||||
chr1:115089462-115089622 | Common:3; Rare:61 | ||||
chr1:116373109-116373348 | Rare:79 | ||||
chr1:116667672-116667884 | Common:2; Rare:75 | ||||
chr1:117060060-117060359 | Common:6; Rare:80 | ||||
chr1:117929568-117929782 | Common:1; Rare:66 | ||||
chr1:119140629-119140748 | Rare:37 | ||||
chr1:120176428-120176621 | Common:1; Rare:44 | ||||
chr1:121184679-121185022 | Common:3; Rare:111 | ||||
chr1:144461625-144461909 | Common:2; Rare:93 | ||||
chr1:145823885-145824280 | Rare:141 | ||||
chr1:145918680-145919034 | Common:2; Rare:80 | ||||
chr1:145927419-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:145964540-145964731 | Rare:48 |