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Using vcftools to find # mappable positions and # of segregating polymorphisms sites

I just installed vcftools and I'm trying to find a way to use it to tell me the # of mappable positions and # of segregating bi-allelic polymorphism sites. Does anybody know how to do this?

The vcf file I'm using is from the 1000 genomes project: ftp://ftp-trace.ncbi.nih.gov/1000genomes/ftp/release/20110521/ALL.chr21.phase1_release_v3.20101123.snps_indels_svs.genotypes.vcf.gz

vcf snp polymorphism

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