Entering edit mode
I have a feeling dbSNP don't archive old releases (see http://www.ncbi.nlm.nih.gov/books/NBK44443/). I'm also quite sure that there's an entry in the VCF (dbSNPBuildID) which shows you which release a variation has been added, so you can parse this information by selecting variants that are in release 126 and before.
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Thank you for your answer. In that case I think it might be easier for me to liftover the hapmap data to hg19 since most population tools out there are geared towards 100 Genomes and already have the supporting data available for hg19 build.