Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:153670909-153671177 | Rare:80 | ||||
chr1:153727786-153728082 | Common:1; Rare:85 | ||||
chr1:153728379-153728596 | Rare:40 | ||||
chr1:153775219-153775274 | Rare:19 | ||||
chr1:153963469-153963715 | Common:2; Rare:67 | ||||
chr1:153967301-153967512 | Common:1; Rare:43 | ||||
chr1:153967624-153967937 | Common:1; Rare:57 | ||||
chr1:153986192-153986449 | Rare:68 | ||||
chr1:154182986-154183305 | Rare:101 | ||||
chr1:154219880-154220221 | Common:5; Rare:87 | ||||
chr1:154220509-154220995 | Common:1; Rare:163 | ||||
chr1:154272266-154272746 | Common:6; Rare:113; Clinvar:2; Clinvar (benign):3 | ||||
chr1:154627864-154628039 | Common:3; Rare:88 | ||||
chr1:154936692-154936762 | Common:1; Rare:20 | ||||
chr1:154956085-154956278 | Common:1; Rare:56 |