Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145927415-145927627 | Common:1; Rare:58; Clinvar (pathogenic):1 | ||||
chr1:145964573-145964749 | Rare:44 | ||||
chr1:147172429-147172830 | Common:1; Rare:103 | ||||
chr1:149886664-149886932 | Rare:80 | ||||
chr1:149887952-149888215 | Rare:57 | ||||
chr1:150067665-150067795 | Rare:34 | ||||
chr1:150364550-150364709 | Common:1; Rare:55 | ||||
chr1:150579595-150579892 | Common:10; Rare:93 | ||||
chr1:150629541-150629827 | Rare:56 | ||||
chr1:151165851-151166162 | Common:3; Rare:87 | ||||
chr1:151190134-151190310 | Rare:51 | ||||
chr1:151198422-151198607 | Common:1; Rare:63 | ||||
chr1:151254678-151254785 | Rare:30 | ||||
chr1:153612957-153613303 | Common:1; Rare:69 | ||||
chr1:153616237-153616474 | Common:1; Rare:41 |