Analyzing differentially methylated regions from Nanopore long read data?

Question

[Arton]

I have a list of differentially methylated regions obtained from Nanopore long-read data. How can I verify the accuracy of the results to ensure the tools performed properly? Additionally, what would be the best approach to analyze a list of differentially methylated regions (proband versus mother, proband versus father)? I would greatly appreciate any ideas or suggestions.