- Description
- Identifies DNA features and regulatory elements in non-coding regions of the human genome. One can enter dbSNP IDs, BED files, VCF files, or GFF3 files. A score is returned assessing the evidence for regulatory potential. Clicking on the score reveals the data supporting the inference, by data type and cell type. One can also click on hyperlinks to see the SNP or the region in the UCSC browser, ENSEMBL browser, and dbSNP.
- Software type
- database, variant annotation
- Used for
- community resource