Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:32222294-32222583 | Rare:117 | ||||
chr1:32291812-32292336 | Common:1; Rare:138 | ||||
chr1:32329292-32329721 | Rare:73 | ||||
chr1:32331367-32331805 | Common:1; Rare:123 | ||||
chr1:32336235-32336504 | Rare:88 | ||||
chr1:32351377-32351635 | Common:1; Rare:66 | ||||
chr1:32394403-32394708 | Common:1; Rare:86 | ||||
chr1:32650921-32651318 | Common:2; Rare:150 | ||||
chr1:32817240-32817699 | Common:1; Rare:123; Clinvar:5; Clinvar (benign):2 | ||||
chr1:32895303-32895923 | Common:2; Rare:200 | ||||
chr1:32901221-32901529 | Common:1; Rare:80 | ||||
chr1:33021369-33021704 | Rare:82; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:33080992-33081179 | Common:2; Rare:48 | ||||
chr1:34985268-34985370 | Common:1; Rare:41 | ||||
chr1:35031648-35031780 | Rare:41 |