Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117367323-117367490 | Common:4; Rare:58 | ||||
chr1:117929560-117929782 | Common:1; Rare:67 | ||||
chr1:119140640-119140677 | Rare:18 | ||||
chr1:120176350-120176614 | Common:1; Rare:55 | ||||
chr1:121184846-121185088 | Rare:84 | ||||
chr1:145823866-145824259 | Rare:136 | ||||
chr1:145858994-145859163 | Rare:47 | ||||
chr1:145918676-145919013 | Common:2; Rare:76; Clinvar:1 | ||||
chr1:145927370-145927600 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
chr1:145957983-145958223 | Rare:57 | ||||
chr1:145964587-145964742 | Rare:37 | ||||
chr1:145994213-145994230 | Rare:5 | ||||
chr1:145994236-145994334 | Rare:39 | ||||
chr1:145995142-145995479 | Rare:131 | ||||
chr1:145995987-145996285 | Rare:134 |