Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153986184-153986403 | Rare:54 | ||||
chr1:153990654-153990814 | Common:2; Rare:74 | ||||
chr1:154182986-154183258 | Rare:89 | ||||
chr1:154220515-154221016 | Common:1; Rare:169 | ||||
chr1:154272503-154272786 | Common:4; Rare:78; Clinvar:3; Clinvar (benign):3 | ||||
chr1:154627910-154628039 | Common:2; Rare:66 | ||||
chr1:154868062-154868092 | Rare:4 | ||||
chr1:154870230-154870315 | Rare:22 | ||||
chr1:154956085-154956235 | Common:1; Rare:42 | ||||
chr1:154961693-154962041 | Common:1; Rare:123 | ||||
chr1:154970716-154970908 | Common:1; Rare:41 | ||||
chr1:154974370-154974717 | Rare:88 | ||||
chr1:154983148-154983388 | Common:2; Rare:47 | ||||
chr1:155127588-155127876 | Common:1; Rare:52 | ||||
chr1:155135737-155135892 | Common:1; Rare:63 |