Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:30879168-30879622 | Common:1; Rare:82 | ||||
chr1:30880649-30881037 | Common:1; Rare:67 | ||||
chr1:30881496-30881543 | Common:1; Rare:17 | ||||
chr1:31065636-31065931 | Common:1; Rare:107 | ||||
chr1:31296720-31297153 | Common:5; Rare:135 | ||||
chr1:32072799-32073001 | Rare:59 | ||||
chr1:32179555-32179768 | Common:1; Rare:52 | ||||
chr1:32179947-32180122 | Rare:51 | ||||
chr1:32291812-32292177 | Common:1; Rare:101 | ||||
chr1:32394410-32394680 | Common:1; Rare:74 | ||||
chr1:32650907-32651318 | Common:2; Rare:151 | ||||
chr1:32651643-32651949 | Rare:77 | ||||
chr1:32817233-32817674 | Rare:116; Clinvar:5 | ||||
chr1:33036772-33037105 | Common:1; Rare:129; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:33080994-33081158 | Common:1; Rare:38 |