Enter or upload a list of mutation identifiers to obtain the total number of mutation pairs, the number of mutation pairs that are associated with the same disease or phenotype, and the number of mutation pairs across interacting chromatin regions. Each mutation identifier entered can be one of the following:
- dbSNP rs ID: e.g. rs669
- Chromosome:position, in hg19: e.g. chr1:167865871
Each mutation identifier should take a new line. You could also upload a text file with all the mutation identifiers. The results of all the mutation pairs associated with the same disease as well as all mutation pairs across interacting chromatin regions will be available for download. Numbers adjacent to the links indicate the fraction of mutation pairs associated with the same disease or across interacting chromatin regions.