Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62625322-62625597 | Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
chr1:63320699-63320934 | Common:1; Rare:35 | ||||
chr1:63320945-63321360 | Common:2; Rare:87 | ||||
chr1:63321573-63321771 | Rare:39 | ||||
chr1:63321845-63322000 | Rare:28 | ||||
chr1:63323727-63323820 | Rare:27 | ||||
chr1:63324677-63324804 | Rare:28 | ||||
chr1:63573647-63573948 | Common:3; Rare:51 | ||||
chr1:63779464-63779536 | Rare:14 | ||||
chr1:64143439-64143714 | Rare:47 | ||||
chr1:64469792-64470226 | Common:2; Rare:94 | ||||
chr1:64471890-64472191 | Common:1; Rare:48 | ||||
chr1:64472405-64472433 | Rare:4 | ||||
chr1:65057844-65058308 | Common:1; Rare:84 | ||||
chr1:65067693-65067753 | Rare:8 |