SRX252751 GSM1102658_1 SRP019829 GSE45338 SRS403016 ChIP-Seq GENOMIC ChIP Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1102658 gds 301102658 GEO Accession GSM1102658 SRX252752 GSM1102659_1 SRP019829 GSE45338 SRS403017 ChIP-Seq GENOMIC ChIP Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1102659 gds 301102659 GEO Accession GSM1102659 SRX252756 GSM1102663_1 SRP019829 GSE45338 SRS403021 RNA-Seq TRANSCRIPTOMIC cDNA AB SOLiD System 3.0 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1102663 gds 301102663 GEO Accession GSM1102663 SRX252757 GSM1102664_1 SRP019829 GSE45338 SRS403022 RNA-Seq TRANSCRIPTOMIC cDNA Illumina Genome Analyzer II GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1102664 gds 301102664 GEO Accession GSM1102664 SRX992415 GSM1656167 SRP019829 SRS907133 GSM1656167 ChIP-Seq GENOMIC ChIP Cells were scraped off dishes and collected by centrifuge. Cross-linked chromatin complexes were isolated from the Nuclei lysis buffer and then sonicated to obtain fragments in a size range between 350-500bp. H3R26Cit antibody (ab19847) were incubated with solubilized DNA fragments overnight at 4°C. Protein A/G agarose beads (Pierce, Rockford, IL) were used to capture the antibody-chromatin complex followed by washes and elution with 1% SDS. The DNA was recovered by reversing the cross-links with 20 mM NaCl at 65°C overnight. DNA was purified by QIAquick PCR Purification Kit (Qiagen 28106) and dissolving in a final volume of 30ul per immunoprecipitation. The Protocol of KAPA High-Throughput Library Preparation Kit (Cat. No. KK8234) Illumina HiSeq 2500 GEO Sample GSM1656167 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1656167 gds 301656167 GEO Accession GSM1656167 SRX2416683 GSM2425393 SRP019829 SRS1854247 GSM2425393 ChIP-Seq GENOMIC ChIP Cells were scraped off dishes and collected by centrifuge. Cross-linked chromatin complexes were isolated from the Nuclei lysis buffer and then sonicated to obtain fragments in a size range between 350-500bp. H3R26Cit antibody (ab19847) were incubated with solubilized DNA fragments overnight at 4°C. Protein A/G agarose beads (Pierce, Rockford, IL) were used to capture the antibody-chromatin complex followed by washes and elution with 1% SDS. The DNA was recovered by reversing the cross-links with 20 mM NaCl at 65°C overnight. DNA was purified by QIAquick PCR Purification Kit (Qiagen 28106) and dissolving in a final volume of 30ul per immunoprecipitation. The Protocol of KAPA High-Throughput Library Preparation Kit (Cat. No. KK8234) Illumina HiSeq 2500 gds 302425393 GEO Accession GSM2425393 SRX2416684 GSM2425394 SRP019829 SRS1854248 GSM2425394 ChIP-Seq GENOMIC ChIP Cells were scraped off dishes and collected by centrifuge. Cross-linked chromatin complexes were isolated from the Nuclei lysis buffer and then sonicated to obtain fragments in a size range between 350-500bp. H3R26Cit antibody (ab19847) were incubated with solubilized DNA fragments overnight at 4°C. Protein A/G agarose beads (Pierce, Rockford, IL) were used to capture the antibody-chromatin complex followed by washes and elution with 1% SDS. The DNA was recovered by reversing the cross-links with 20 mM NaCl at 65°C overnight. DNA was purified by QIAquick PCR Purification Kit (Qiagen 28106) and dissolving in a final volume of 30ul per immunoprecipitation. The Protocol of KAPA High-Throughput Library Preparation Kit (Cat. No. KK8234) Illumina HiSeq 2500 gds 302425394 GEO Accession GSM2425394 SRX2416685 GSM2425395 SRP019829 SRS1854249 GSM2425395 ChIP-Seq GENOMIC ChIP Cells were scraped off dishes and collected by centrifuge. Cross-linked chromatin complexes were isolated from the Nuclei lysis buffer and then sonicated to obtain fragments in a size range between 350-500bp. H3R26Cit antibody (ab19847) were incubated with solubilized DNA fragments overnight at 4°C. Protein A/G agarose beads (Pierce, Rockford, IL) were used to capture the antibody-chromatin complex followed by washes and elution with 1% SDS. The DNA was recovered by reversing the cross-links with 20 mM NaCl at 65°C overnight. DNA was purified by QIAquick PCR Purification Kit (Qiagen 28106) and dissolving in a final volume of 30ul per immunoprecipitation. The Protocol of KAPA High-Throughput Library Preparation Kit (Cat. No. KK8234) Illumina HiSeq 2500 gds 302425395 GEO Accession GSM2425395 SRX2416686 GSM2425396 SRP019829 SRS1854250 GSM2425396 ChIP-Seq GENOMIC ChIP Cells were scraped off dishes and collected by centrifuge. Cross-linked chromatin complexes were isolated from the Nuclei lysis buffer and then sonicated to obtain fragments in a size range between 350-500bp. H3R26Cit antibody (ab19847) were incubated with solubilized DNA fragments overnight at 4°C. Protein A/G agarose beads (Pierce, Rockford, IL) were used to capture the antibody-chromatin complex followed by washes and elution with 1% SDS. The DNA was recovered by reversing the cross-links with 20 mM NaCl at 65°C overnight. DNA was purified by QIAquick PCR Purification Kit (Qiagen 28106) and dissolving in a final volume of 30ul per immunoprecipitation. The Protocol of KAPA High-Throughput Library Preparation Kit (Cat. No. KK8234) Illumina HiSeq 2500 gds 302425396 GEO Accession GSM2425396 SRX2416687 GSM2425397 SRP019829 SRS1854251 GSM2425397 ChIP-Seq GENOMIC ChIP Cells were scraped off dishes and collected by centrifuge. Cross-linked chromatin complexes were isolated from the Nuclei lysis buffer and then sonicated to obtain fragments in a size range between 350-500bp. H3R26Cit antibody (ab19847) were incubated with solubilized DNA fragments overnight at 4°C. Protein A/G agarose beads (Pierce, Rockford, IL) were used to capture the antibody-chromatin complex followed by washes and elution with 1% SDS. The DNA was recovered by reversing the cross-links with 20 mM NaCl at 65°C overnight. DNA was purified by QIAquick PCR Purification Kit (Qiagen 28106) and dissolving in a final volume of 30ul per immunoprecipitation. The Protocol of KAPA High-Throughput Library Preparation Kit (Cat. No. KK8234) Illumina HiSeq 2500 gds 302425397 GEO Accession GSM2425397 SRX2416688 GSM2425398 SRP019829 SRS1854252 GSM2425398 ChIP-Seq GENOMIC ChIP Cells were scraped off dishes and collected by centrifuge. Cross-linked chromatin complexes were isolated from the Nuclei lysis buffer and then sonicated to obtain fragments in a size range between 350-500bp. H3R26Cit antibody (ab19847) were incubated with solubilized DNA fragments overnight at 4°C. Protein A/G agarose beads (Pierce, Rockford, IL) were used to capture the antibody-chromatin complex followed by washes and elution with 1% SDS. The DNA was recovered by reversing the cross-links with 20 mM NaCl at 65°C overnight. DNA was purified by QIAquick PCR Purification Kit (Qiagen 28106) and dissolving in a final volume of 30ul per immunoprecipitation. The Protocol of KAPA High-Throughput Library Preparation Kit (Cat. No. KK8234) Illumina HiSeq 2500 gds 302425398 GEO Accession GSM2425398 SRX2416689 GSM2425399 SRP019829 SRS1854253 GSM2425399 RNA-Seq TRANSCRIPTOMIC cDNA Cells were scraped off dishes and collected by centrifuge. Cross-linked chromatin complexes were isolated from the Nuclei lysis buffer and then sonicated to obtain fragments in a size range between 350-500bp. H3R26Cit antibody (ab19847) were incubated with solubilized DNA fragments overnight at 4°C. Protein A/G agarose beads (Pierce, Rockford, IL) were used to capture the antibody-chromatin complex followed by washes and elution with 1% SDS. The DNA was recovered by reversing the cross-links with 20 mM NaCl at 65°C overnight. DNA was purified by QIAquick PCR Purification Kit (Qiagen 28106) and dissolving in a final volume of 30ul per immunoprecipitation. The Protocol of KAPA High-Throughput Library Preparation Kit (Cat. No. KK8234) Illumina HiSeq 2500 gds 302425399 GEO Accession GSM2425399 SRX2416690 GSM2425400 SRP019829 SRS1854254 GSM2425400 RNA-Seq TRANSCRIPTOMIC cDNA Cells were scraped off dishes and collected by centrifuge. Cross-linked chromatin complexes were isolated from the Nuclei lysis buffer and then sonicated to obtain fragments in a size range between 350-500bp. H3R26Cit antibody (ab19847) were incubated with solubilized DNA fragments overnight at 4°C. Protein A/G agarose beads (Pierce, Rockford, IL) were used to capture the antibody-chromatin complex followed by washes and elution with 1% SDS. The DNA was recovered by reversing the cross-links with 20 mM NaCl at 65°C overnight. DNA was purified by QIAquick PCR Purification Kit (Qiagen 28106) and dissolving in a final volume of 30ul per immunoprecipitation. The Protocol of KAPA High-Throughput Library Preparation Kit (Cat. No. KK8234) Illumina HiSeq 2500 gds 302425400 GEO Accession GSM2425400