Currently I am working on variation related to different vitamins. I have collected details from UCSC genome browser with the genome assembly GRCh37/hg19, All SNPs (141) and I need to use these data got from UCSC in dbSNP but my question is that, will the dbSNP 141 and GRCh37/hg19, All SNPs (141) provide similar data or are they same? My second question is that, is it possible to find information about CpG islands, miRNA, CNVs from Ensembl? If can, how?
I will be grateful if any one help me to clear my doubt. Please help me soon.....