When users input a genomic region, VARAdb will identify variations and enhancer
overlapping with the submitted region.
1)Enhancer type: Types of enhancer including active enhancer, disease enhancer,super enhancer, typical enhancer and validated enhancer.
2)Source: Source of enhancer.
Number of records of different enhancer sources
Transcription factors distribution
Please choose one 'data type' and a data source firstly, then provide a disease or
phenotype name. The VARAdb will show variations of the disease/trait/phenotype
1)Data type: Users can choose one type including eQTL, GWAS and variant disease association information.
2)Data source: Users can select a source about the data type.
3)Disease/trait/phenotype: Users can provide a disease/trait/phenotype name of interest.
Number of records of different disease/trait/phenotype sources
When users input a gene name,VARAdb will identify variations associated with the gene. Note that the gene is one of the eQTL genes,gwas reported genes or the closest gene of variation.
1)Gene:Gene Symbol/Ensembl ID/NCBI Refseq ID/Alias/Entrez Gene ID