Haplotype-Specific DNA Methylation
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MIR675
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rs4930103
chr11:2024543-2024544
genes 2
GWAS disease/phenotype 2
rs4930103
LD Block:
chr11:1866371-2040997
Genes:
H19
MIR675
GWAS Disease/Phenotype:
DNA methylation (parent-of-origin)
DNA methylation (variation)
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