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In present research, the two haplotypes with deep divergence tend to be described by examining 1000 genomes task information and observed becoming with a high frequencies in every human populations. Through populace genetics analysis and genome annotation, the potential useful region is identified and verified by reporter gene assay. Further mutagenesis shows that the useful mutations tend to be rs66862535 and rs68096061. Both SNPs can modify the discussion performance of transcript

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