Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114780558-114780785 | Common:1; Rare:86 | ||||
chr1:115976805-115976884 | Rare:20 | ||||
chr1:117929568-117929795 | Common:1; Rare:68 | ||||
chr1:119140640-119140785 | Common:1; Rare:45 | ||||
chr1:120176354-120176614 | Common:1; Rare:55 | ||||
chr1:120914108-120914204 | Rare:9 | ||||
chr1:145823885-145824312 | Rare:148 | ||||
chr1:145858996-145859165 | Rare:47 | ||||
chr1:145918676-145919034 | Common:2; Rare:82; Clinvar:1 | ||||
chr1:145927370-145927648 | Common:1; Rare:72; Clinvar (pathogenic):1 | ||||
chr1:145964542-145964754 | Rare:54 | ||||
chr1:146938297-146938343 | Rare:21 | ||||
chr1:147172420-147172786 | Common:1; Rare:94 | ||||
chr1:147541406-147541501 | Rare:12 | ||||
chr1:147928254-147928472 | Common:2; Rare:76 |