Research
Non-imprinted allele-specific DNA methylation on human autosomes
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* Corresponding author: Albert Jeltsch a.jeltsch@jacobs-university.de
1 School of Engineering and Science, Jacobs University Bremen, Campus Ring 1, D-28759 Bremen, Germany
2 Max Planck Institute for Molecular Genetics, Ihnestrasse 63-73, D-14195 Berlin-Dahlem, Germany
3 Jacobs Center on Lifelong Learning and Institutional Development, Jacobs University Bremen, Campus Ring 1, D-28759 Bremen, Germany
Genome Biology 2009, 10:R138 doi:10.1186/gb-2009-10-12-r138
Published: 3 December 2009Additional files
Additional data file 1:
Amplicons analyzed and the correlated genes, genomic positions and primers used for bisulfite genomic sequencing and gene expression analysis.
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Additional data file 2:
Detailed information for all individuals selected for the analysis.
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Additional data file 3:
Confirmation of the bisulfite genomic sequencing results.
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Additional data file 4:
DNA methylation patterns of amplicons 23_1 and 23_2 in different individuals.
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Additional data file 5:
DNA methylation patterns of amplicon 262 in different individuals.
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Additional data file 6:
Methylation levels of homozygous individuals compared with the allelic methylation levels of heterozygous individuals for amplicons 23_1, 23_2 and 262.
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Additional data file 7:
Methylation patterns of amplicon 232 in different individuals.
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Additional data file 8:
ASM of amplicons 176_1 and 176_2.
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Additional data file 9:
Methylation levels of regions with ASM in HEK293 cells, HEPG2 cells and human fibroblasts from [12].
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Additional data file 10:
Allele-specific transcription factor binding sites predicted at the ASM amplicons and mechanism of ASM.
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