TOAnnoPriDB
an integrative Database for Trans-Omic Annotation and Prioritization of non-coding variants across human genome

Trans-Omic Analyse Variants


Analyse any variants across human genome. Analyse a single variant, multiple variants, or a vcf file were surported.



Single variant analysis: 
Chromosome:   Start:   End:   Ref:   Alt:  

Example: Chromosome:chr8; Start:101073779; End:101073779; Ref:A; Alt:G, Chromosome:chr11; Start:31664675; End:31664677; Ref:ATTC; Alt:A



Multiple variants analysis: 
List of variants:    

Example: chr11:31509761-31509761:T>C; chr11:31509774-31509774:G>T; chr11:31509779-31509779:T>G



File analysis: 
Upload a file:

* Please upload a tab-separated file in BED format including the chromosome, start position, end position, ref allele, and alt allele of each variant.
  If the file containing more than 50 lines, only the first 50 variats will be analyzed.

© 2022. Center for Big Data Research in Health, Key Laboratory of Epigenetic Regulation and Intervention, Institute of Biophysics, Chinese Academy of Sciences