Enter dbSNP IDs, 0-based coordinates, BED files, VCF files, GFF3 files (hg19).

Use RegulomeDB to identify DNA features and regulatory elements in non-coding regions of the human genome by entering ...

Enter dbSNP ID(s) (example) or upload a list of dbSNP IDs to identify DNA features and regulatory elements that contain the coordinate of the SNP(s).
Enter hg19 coordinates for a single nucleotide as 0-based (example) coordinates or in a BED file (example), VCF file (example), or GFF3 file (example). These coordinates will be mapped to a dbSNP IDs (if available) in addition to identifying DNA features and regulatory elements that contain the input coordinate(s).
Enter hg19 chromosomal regions, such as a promoter region upstream of a gene, as 0-based (example) coordinates or in a BED file (example) or GFF3 file (example). All dbSNP IDs with an allele frequency >1% that are found in this region will be used to identify DNA features and regulatory elements that contain the coordinate of the SNP(s).
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