We have generated the whole genome variation map for all 705 accessions. However, it is difficult to search the genetic variants between two accessions from the huge data. Here we present a convenient searching method to get the genome variations. Only the ID of two accessions was needed to be input into the blank to get the genetic variants in CSV format.
Eg: You can input G001 and G002 to get genetic variants between the two accessions in the whole genome level(Only the capital "G" could be used).