Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:120069594-120069920 | Common:7; Rare:68 | ||||
chr1:120176350-120176684 | Common:1; Rare:61 | ||||
chr1:145823891-145824249 | Rare:128 | ||||
chr1:145858996-145859167 | Rare:48 | ||||
chr1:145918689-145919013 | Common:2; Rare:69 | ||||
chr1:145927394-145927634 | Common:1; Rare:63; Clinvar (pathogenic):1 | ||||
chr1:145957974-145958223 | Rare:60 | ||||
chr1:145964559-145964742 | Rare:47 | ||||
chr1:146228968-146229190 | Common:2; Rare:46 | ||||
chr1:147172427-147172786 | Common:1; Rare:93 | ||||
chr1:147225303-147225555 | Common:3; Rare:49 | ||||
chr1:147242500-147242715 | Common:3; Rare:77 | ||||
chr1:148679740-148679929 | Rare:17 | ||||
chr1:148844339-148844432 | Rare:8 | ||||
chr1:148952273-148952603 | Common:5; Rare:99 |