Hello Amal,
Thank you for your question about converting kpg ID numbers into dbSNP rsID numbers. There are a couple of ways for you to do this. One is to convert the locations of your kpg items into a BED file and use that to filter our dbSNP track. More information about how to do that is available in the answer to this mailing list question: https://groups.google.com/a/soe.ucsc.edu/d/topic/genome/0pM24K2BrYs/discussion. Alternatively, if it is easier, you can convert your variants into pgSNP format (http://genome.ucsc.edu/FAQ/FAQformat.html#format10) and pass them as input into the Variant Annotation Integrator (http://genome.ucsc.edu/cgi-bin/hgVai). The VAI tool has an option to automatically list any known dbSNP variants that match its input. More information about how to do this is available at https://groups.google.com/a/soe.ucsc.edu/d/topic/genome/Rx4v-f5QVYI/discussion.
I hope this is helpful. If you have any further questions, please reply to gen...@soe.ucsc.edu or genome...@soe.ucsc.edu. Questions sent to those addresses will be archived in publicly-accessible forums for the benefit of other users. If your question contains sensitive data, you may send it instead to genom...@soe.ucsc.edu.
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Jonathan Casper
UCSC Genome Bioinformatics Group
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