Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:115089472-115089610 | Common:2; Rare:50 | ||||
chr1:116570960-116571197 | Common:2; Rare:69 | ||||
chr1:117060062-117060368 | Common:6; Rare:87 | ||||
chr1:117367297-117367516 | Common:5; Rare:81 | ||||
chr1:117929593-117929839 | Common:3; Rare:71 | ||||
chr1:119140610-119140771 | Common:1; Rare:55 | ||||
chr1:120176310-120176552 | Rare:52 | ||||
chr1:121184714-121184996 | Common:2; Rare:93 | ||||
chr1:145773498-145773862 | Common:4; Rare:53 | ||||
chr1:145823895-145824249 | Rare:126 | ||||
chr1:145836309-145836578 | Rare:65 | ||||
chr1:145858976-145859205 | Rare:66 | ||||
chr1:145918621-145919054 | Common:2; Rare:105; Clinvar:2 | ||||
chr1:145925794-145926138 | Common:2; Rare:103; Clinvar:1 | ||||
chr1:145927313-145927644 | Common:1; Rare:90; Clinvar (pathogenic):2 |