Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161118000-161118141 | Rare:73 | ||||
chr1:161132356-161132709 | Common:1; Rare:109 | ||||
chr1:161153732-161153824 | Rare:22 | ||||
chr1:161159404-161159532 | Common:1; Rare:37 | ||||
chr1:161166268-161166512 | Common:2; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
chr1:161225745-161226069 | Common:10; Rare:49 | ||||
chr1:161314265-161314425 | Common:3; Rare:65; Clinvar:9; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161749763-161749829 | Rare:30 | ||||
chr1:161750214-161750239 | Rare:6 | ||||
chr1:161750264-161750441 | Rare:33 | ||||
chr1:161766198-161766371 | Common:3; Rare:58 | ||||
chr1:162497707-162497862 | Common:2; Rare:46 | ||||
chr1:162561346-162561609 | Common:3; Rare:103 | ||||
chr1:162790516-162790800 | Common:4; Rare:85 | ||||
chr1:163202824-163203289 | Common:1; Rare:88 |