Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154220513-154220978 | Common:1; Rare:156 | ||||
chr1:154272503-154272773 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):3 | ||||
chr1:154627882-154628035 | Common:3; Rare:79 | ||||
chr1:154936627-154936762 | Common:2; Rare:45 | ||||
chr1:154936842-154937016 | Rare:33 | ||||
chr1:154956085-154956235 | Common:1; Rare:42 | ||||
chr1:154961712-154962059 | Common:1; Rare:118 | ||||
chr1:154968208-154968543 | Rare:84 | ||||
chr1:154970050-154970337 | Common:1; Rare:85 | ||||
chr1:154970703-154970908 | Common:1; Rare:44 | ||||
chr1:154974327-154974751 | Rare:111 | ||||
chr1:154983128-154983393 | Common:2; Rare:53; Clinvar (benign):1 | ||||
chr1:155051159-155051389 | Common:1; Rare:78 | ||||
chr1:155135703-155135905 | Common:3; Rare:88 | ||||
chr1:155209165-155209266 | Rare:41 |