Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116373945-116374090 | Common:1; Rare:48 | ||||
chr1:116399236-116399510 | Rare:45 | ||||
chr1:116754351-116754467 | Rare:34 | ||||
chr1:117929546-117929800 | Common:2; Rare:75 | ||||
chr1:118987879-118988385 | Common:1; Rare:129 | ||||
chr1:119140619-119140782 | Common:1; Rare:56 | ||||
chr1:119648125-119648367 | Common:3; Rare:81 | ||||
chr1:120176343-120176656 | Common:1; Rare:59 | ||||
chr1:121184818-121185088 | Rare:93 | ||||
chr1:145823827-145824078 | Rare:98 | ||||
chr1:145824081-145824279 | Rare:64 | ||||
chr1:145858996-145859175 | Rare:51 | ||||
chr1:145918686-145919013 | Common:2; Rare:70 | ||||
chr1:145927364-145927632 | Common:1; Rare:68; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958223 | Rare:52 |