Related Experiment Video
Updated: Feb 18, 2026

Sample Preparation to Bioinformatics Analysis of DNA Methylation: Association Strategy for Obesity and Related Trait Studies
Published on: May 6, 2022
SNP in Differentially Methylated Region Upstream of H19 Gene in Guangdong Han Population
1Key Laboratory of Reproduction and Genetics of Guangdong Higher Education Institutes, Institute of Forensic Identification, the Third Affiliated Hospital of Guangzhou Medical University, Guangdong 510150, China.
Objectives:
To investigate the single nucleotide polymorphism (SNP) and haplotypes in differentially methylated region (DMR) upstream of H19 gene in Guangdong Han population.
Methods:
The PIA typing and restriction enzyme McrBC and HpaⅡ were used to digest the genomic DNA and obtain the individual uniparental DNA template strand. The data of uniparental SNP alleles, genotypes and haplotypes in DMR upstream of H19 gene were obtained by sequencing.
Results:
A total of 13 SNPs (rs10840167, rs2525883, rs12417375, rs4930101, rs2525882, rs2735970, rs2735971, rs11042170, rs2735972, rs10732516, rs2071094, rs2107425, and rs4930098) and one mutation locus (g7351c) were found. All loci followed the Hardy-Weinberg equilibrium (P>0.05) by statistical analysis. Except for rs12417375 (DP=0.279) locus, the DP of remaining 12 SNPs were 0.446-0.614, and the g7351c mutation locus (DP=0.013) was the particular loci of the Southern Chinese Han population. Eight haplotypes (designated as haplotype 1-8) were detected, in which 3 haplotypes had not yet been reported and the DP, PIC, PE and H were 0.891, 0.714, 0.524 and 0.758, respectively.
Conclusions:
Obtained by PIA typing, the SNP in DMR upstream of H19 gene and its haplotypes genetic marker system have a high determination power and show a good practical value in forensic identification.
Related Concept Videos
Single Nucleotide Polymorphisms-SNPs
Genome-wide Association Studies-GWAS
GWAS does not require the identification of the target gene involved in...
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

