Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161153736-161154073 | Common:1; Rare:101; Clinvar (pathogenic):1 | ||||
chr1:161159392-161159532 | Common:1; Rare:40 | ||||
chr1:161166257-161166726 | Common:4; Rare:115; Clinvar:5; Clinvar (benign):2 | ||||
chr1:161199018-161199253 | Rare:35 | ||||
chr1:161223329-161223757 | Common:1; Rare:105; Clinvar:2 | ||||
chr1:161225768-161226078 | Common:10; Rare:44 | ||||
chr1:161238094-161238388 | Common:1; Rare:43 | ||||
chr1:161258600-161258786 | Common:2; Rare:40 | ||||
chr1:161314327-161314425 | Common:2; Rare:43; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161549670-161549894 | Common:1; Rare:86 | ||||
chr1:161631112-161631375 | Common:8; Rare:99 | ||||
chr1:161749756-161749829 | Rare:31 | ||||
chr1:161750210-161750294 | Rare:27 | ||||
chr1:161766164-161766570 | Common:5; Rare:116; Clinvar (pathogenic):1 | ||||
chr1:162069558-162069753 | Common:1; Rare:51 |