To view the position of the amplicons for each target, download the panel output zip file from the panel details page. Once downloaded, extract the contents of the zip file. Use the interface within the UCSC Genome Browser to overlay the tracks to display the coverage of the SNP databases.
Add custom tracks into the browser using the "Custom Tracks" command in the "My Data" menu. This can be used to load the submitted.bed, missed.bed, insert.bed and amplicons.bed file found in the designer zip to help visualize where the primers are in relation to targets.
The target regions submitted to Tapestri Designer are shown in blue. The areas covered by the inserts are in green. The target regions not covered by the panel (assuming 2x150 bp sequencing) are in red. For more information on missed targets view this article.
Source: genome.ucsc.edu
Custom panels built on UCSC genomes can be visualized, but the .bed files may need to be edited such that the db field matches the UCSC genome name. In the example below, hg19_chrM would need to be changed to hg19.