We have CLC Genomics in the lab for CMV variants analysis but i am no longer using it. you can contact https://www.researchgate.net/profile/Raphaelle_Riou for help
There are several ways you can try to collect the information under CLC. There is a "Create Statistics for Target Regions" tool under "Resequencing Analysis", but you need to first create a target region file to use the tool; it is very handy for genome with large size and large number of target region. Alternatively, as shown in your figure, with short region and a few target regions, you can just right click on your coverage track and "Export Graph to Comma-separated File" and it will give you the coverage on each base where you can extract the information you need.