Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116667674-116667857 | Common:1; Rare:67 | ||||
chr1:117605780-117606057 | Rare:80 | ||||
chr1:117929568-117929806 | Common:4; Rare:71 | ||||
chr1:119140597-119140776 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
chr1:119648131-119648364 | Common:3; Rare:81 | ||||
chr1:121184915-121185022 | Rare:37 | ||||
chr1:145823895-145824251 | Rare:126 | ||||
chr1:145918680-145919022 | Common:2; Rare:79 | ||||
chr1:145927426-145927612 | Common:1; Rare:54; Clinvar (pathogenic):1 | ||||
chr1:145958006-145958202 | Rare:46 | ||||
chr1:145964593-145964742 | Rare:33 | ||||
chr1:145995169-145995463 | Rare:117 | ||||
chr1:145996534-145996790 | Rare:102 | ||||
chr1:146228968-146229167 | Common:2; Rare:46 | ||||
chr1:146938308-146938331 | Rare:11 |