SRX1837288 GSM2197439 SRP076399 SRS1496683 GSM2197439 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197439 GEO Accession GSM2197439 SRX1837289 GSM2197440 SRP076399 SRS1496684 GSM2197440 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197440 GEO Accession GSM2197440 SRX1837290 GSM2197441 SRP076399 SRS1496685 GSM2197441 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197441 GEO Accession GSM2197441 SRX1837291 GSM2197442 SRP076399 SRS1496687 GSM2197442 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197442 GEO Accession GSM2197442 SRX1837292 GSM2197443 SRP076399 SRS1496686 GSM2197443 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197443 GEO Accession GSM2197443 SRX1837293 GSM2197444 SRP076399 SRS1496688 GSM2197444 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197444 GEO Accession GSM2197444 SRX1837296 GSM2197447 SRP076399 SRS1496691 GSM2197447 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197447 GEO Accession GSM2197447 SRX1837297 GSM2197448 SRP076399 SRS1496693 GSM2197448 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197448 GEO Accession GSM2197448 SRX1837298 GSM2197449 SRP076399 SRS1496692 GSM2197449 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197449 GEO Accession GSM2197449 SRX1837299 GSM2197450 SRP076399 SRS1496694 GSM2197450 ChIP-Seq GENOMIC ChIP 100 dissected ovaries were crosslinked with 1.8% formaldehyde for 10 min, and the prepared chromatin was sonicated. One-third was used for immunoprecipitation by H3K9me3 antibody. After decrosslinking, DNA was extracted and used for library preparation for sequencing. The ChIP-seq experiments were performed in three biological replicates. Library preparation and 50nt single-read sequencing were performed by Donnelly Sequencing Centre (Toronto) on an Illumina HiSeq2500. Illumina HiSeq 2500 gds 302197450 GEO Accession GSM2197450