Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117929606-117929848 | Common:3; Rare:64 | ||||
chr1:119140571-119140771 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:119648119-119648386 | Common:3; Rare:87 | ||||
chr1:119711568-119711965 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):2 | ||||
chr1:145773342-145773633 | Rare:56 | ||||
chr1:145823924-145824260 | Rare:116 | ||||
chr1:145918634-145919057 | Common:2; Rare:103; Clinvar:2 | ||||
chr1:145925797-145926138 | Common:2; Rare:102; Clinvar:1 | ||||
chr1:145927333-145927627 | Common:1; Rare:77; Clinvar (pathogenic):1 | ||||
chr1:145957987-145958212 | Rare:52 | ||||
chr1:145964484-145964763 | Rare:62 | ||||
chr1:145996435-145996771 | Common:1; Rare:125 | ||||
chr1:147172429-147172786 | Common:1; Rare:92 | ||||
chr1:147225587-147225906 | Common:8; Rare:49 | ||||
chr1:147541285-147541569 | Common:1; Rare:46 |