SRX6049855 GSM3879725 SRP201233 SRS4969270 GSM3879725 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879725 GSM3879725 GEO Accession GSM3879725 SRX6049856 GSM3879715 SRP201233 SRS4969269 GSM3879715 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879715 GSM3879715 GEO Accession GSM3879715 SRX6049857 GSM3879716 SRP201233 SRS4969271 GSM3879716 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879716 GSM3879716 GEO Accession GSM3879716 SRX6049858 GSM3879717 SRP201233 SRS4969268 GSM3879717 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879717 GSM3879717 GEO Accession GSM3879717 SRX6049859 GSM3879718 SRP201233 SRS4969273 GSM3879718 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879718 GSM3879718 GEO Accession GSM3879718 SRX6049860 GSM3879719 SRP201233 SRS4969274 GSM3879719 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879719 GSM3879719 GEO Accession GSM3879719 SRX6049861 GSM3879720 SRP201233 SRS4969272 GSM3879720 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879720 GSM3879720 GEO Accession GSM3879720 SRX6049862 GSM3879721 SRP201233 SRS4969278 GSM3879721 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879721 GSM3879721 GEO Accession GSM3879721 SRX6049863 GSM3879722 SRP201233 SRS4969276 GSM3879722 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879722 GSM3879722 GEO Accession GSM3879722 SRX6049864 GSM3879723 SRP201233 SRS4969275 GSM3879723 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879723 GSM3879723 GEO Accession GSM3879723 SRX6049865 GSM3879724 SRP201233 SRS4969277 GSM3879724 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879724 GSM3879724 GEO Accession GSM3879724 SRX6049866 GSM3879726 SRP201233 SRS4969279 GSM3879726 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879726 GSM3879726 GEO Accession GSM3879726 SRX6049867 GSM3879727 SRP201233 SRS4969280 GSM3879727 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879727 GSM3879727 GEO Accession GSM3879727 SRX6049868 GSM3879728 SRP201233 SRS4969283 GSM3879728 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879728 GSM3879728 GEO Accession GSM3879728 SRX6049869 GSM3879729 SRP201233 SRS4969281 GSM3879729 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879729 GSM3879729 GEO Accession GSM3879729 SRX6049870 GSM3879730 SRP201233 SRS4969282 GSM3879730 ChIP-Seq GENOMIC ChIP Cells were fixed by adding 1/10 volume of freshly-prepared formaldehyde solution (11% formaldehyde, 0.1 M NaCl, 1 mM EDTA pH 8.0, 50 mM HEPES pH 7.9) to the existing media in each cell culture plate. Plates with added formaldehyde solution were agitated 15 minutes at room temperature. Fixation was stopped by adding 1/20 volume a 2.5 M glycine solution and incubating at room temperature for 5 minutes. Subsequently, cells were scraped off the culture dish surface and washed by transferring to a 50 ml conical tube on ice and pelleting at 800 x g in a refrigerated centrifuge for 10 minutes. Supernatant was removed and cells were re-suspended cells in 10 ml chilled PBS-Igepal (1x PBS pH 7.4, 0.5% Igepal CA-630). Cells were centrifuged again, supernatant was removed, and 10 ml chilled PBS-Igepal supplemented with 1 mM PMSF was added and the cell pellet was resuspemded. Cells were pelleted again at 800 x g, supernatant removed completely, and the cell pellet was snap-frozen on dry ice. Frozen cell pellets were kept at -80C and shipped to Active Motif (AM, commercial service provider) for further processing (chromatin extraction, fragmentation, antibody-precipitation and library preparation) according to AM's standard procedure. Libraries were prepared by Active Motif (Carlsbad, CA) for sequencing using standard Illumina protocols Illumina HiSeq 2000 gds 303879730 GSM3879730 GEO Accession GSM3879730