Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:111755535-111755744 | Common:3; Rare:77 | ||||
chr1:112619096-112619199 | Rare:38 | ||||
chr1:112619643-112619851 | Common:1; Rare:71 | ||||
chr1:112956178-112956437 | Common:4; Rare:116; Clinvar:9; Clinvar (benign):3 | ||||
chr1:113073095-113073247 | Common:1; Rare:58 | ||||
chr1:113905026-113905365 | Common:3; Rare:92 | ||||
chr1:114669991-114670269 | Common:1; Rare:89 | ||||
chr1:117367323-117367559 | Common:5; Rare:78 | ||||
chr1:117929560-117929806 | Common:4; Rare:72 | ||||
chr1:118987575-118987733 | Rare:52 | ||||
chr1:119140640-119140724 | Rare:23 | ||||
chr1:121184907-121185067 | Rare:59 | ||||
chr1:145823827-145824265 | Rare:159 | ||||
chr1:145859668-145859840 | Common:1; Rare:51 | ||||
chr1:145918658-145919042 | Common:2; Rare:94; Clinvar:1 |