# Launching the Chromosome View
The *Chromosome view* can be invoked from some data nodes on the *Analyses* tab, giving a global overview of the results; or from certain *Task report* or result pages, providing a focused view, i.e. pointing to a specific feature of interest.
## Running a Chromosome View Task from a Data Node
On the *Analyses* tab, selecting a data node containing aligned reads, variants, or feature lists, shows *Chromosome view* in the *Exploratory analysis* section of the context-sensitive menu.
If Connected Multiomics has no information on the genome build for the data, you will need to provide the species and genome build in a subsequent dialog (not shown). Otherwise, chromosome view will come up directly.
A new *Chromosome view* task node will be added to the task graph. To invoke the viewer, **double-click** on the node (you can also select it and then go to **Task report** in the menu). When invoked in this way, the default visualization in the *Chromosome view* is the first 100,000 bases of the first chromosome.
## Browsing directly to a location directly from a Task Report
Another way to get the *Chromosome view* is through a *Task report*. You can launch the viewer by selecting the **chromosome icon**  in the View column of differential test report or *View Variants* reports. In that case, the *Chromosome view* will browse directly to the selected genomic location (i.e. a transcript or a variant, depending on the analysis pipeline).
Depending on the task report used to invoke the *Chromosome view* was invoked, some tracks may be pre-selected and customized. For example, when invoked from a variant table, the reads histogram track will be colored by bases (rather than the default of coloring by sample).
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