{{Rsnum
|rsid=10732516
|Chromosome=11
|position=1999976
|Orientation=plus
|GMAF=0.3476
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{PMID Auto
|PMID=21991322
|Title=Impact of the genome on the epigenome is manifested in DNA methylation patterns of imprinted regions in monozygotic and dizygotic twins
|OA=1
}}{{PMID|16839189|OA=1
}} Human imprinted chromosomal regions are historical hot-spots of recombination.

{{PMID|17012269|OA=1
}} Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region.

{{PMID|19936258|OA=1
}} Epigenetic features of human mesenchymal stem cells determine their permissiveness for induction of relevant transcriptional changes by SYT-SSX1.
{{PMID Auto
|PMID=24575294
|Title=Interplay between polymorphisms and methylation in the H19/IGF2 gene region may contribute to obesity in Mexican-American children
|OA=1
}}{{PMID Auto
|PMID=23725790
|Title=GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.
}}