SRX312235 GSM1171652 SRP026218 GSE48176 SRS449834 GSM1171652 ChIP-Seq GENOMIC ChIP Cells were fixed for 10min at RT in 1% formaldehyde, harvested using a cell scraper, washed once in ice-cold PBS, and resuspended in RIPA buffer with protease inhibitor. The sample was then sonicated using an 3.2mm microtip (QSonica Sonicator 4000) at 30s on 30s off intervals and 40% amplitude for 180min while in a -30C 3:1 isopropanol and water bath containing dry ice. Subsequent steps were performed as per the standard protocol. DNA was size-selected during library building to an average fragment size of 200bp. Libraries were sequenced using Illumina HiSeq 2000. Libraries were generated following Illumina's DNA Sample Prep Kit protocol Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1171652 gds 301171652 GEO Accession GSM1171652 SRX312236 GSM1171653 SRP026218 GSE48176 SRS449827 GSM1171653 ChIP-Seq GENOMIC ChIP Cells were fixed for 10min at RT in 1% formaldehyde, harvested using a cell scraper, washed once in ice-cold PBS, and resuspended in RIPA buffer with protease inhibitor. The sample was then sonicated using an 3.2mm microtip (QSonica Sonicator 4000) at 30s on 30s off intervals and 40% amplitude for 180min while in a -30C 3:1 isopropanol and water bath containing dry ice. Subsequent steps were performed as per the standard protocol. DNA was size-selected during library building to an average fragment size of 200bp. Libraries were sequenced using Illumina HiSeq 2000. Libraries were generated following Illumina's DNA Sample Prep Kit protocol Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1171653 gds 301171653 GEO Accession GSM1171653 SRX312237 GSM1171654 SRP026218 GSE48176 SRS449832 GSM1171654 ChIP-Seq GENOMIC ChIP Cells were fixed for 10min at RT in 1% formaldehyde, harvested using a cell scraper, washed once in ice-cold PBS, and resuspended in RIPA buffer with protease inhibitor. The sample was then sonicated using an 3.2mm microtip (QSonica Sonicator 4000) at 30s on 30s off intervals and 40% amplitude for 180min while in a -30C 3:1 isopropanol and water bath containing dry ice. Subsequent steps were performed as per the standard protocol. DNA was size-selected during library building to an average fragment size of 200bp. Libraries were sequenced using Illumina HiSeq 2000. Libraries were generated following Illumina's DNA Sample Prep Kit protocol Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1171654 gds 301171654 GEO Accession GSM1171654 SRX312238 GSM1171655 SRP026218 GSE48176 SRS449829 GSM1171655 ChIP-Seq GENOMIC ChIP Cells were fixed for 10min at RT in 1% formaldehyde, harvested using a cell scraper, washed once in ice-cold PBS, and resuspended in RIPA buffer with protease inhibitor. The sample was then sonicated using an 3.2mm microtip (QSonica Sonicator 4000) at 30s on 30s off intervals and 40% amplitude for 180min while in a -30C 3:1 isopropanol and water bath containing dry ice. Subsequent steps were performed as per the standard protocol. DNA was size-selected during library building to an average fragment size of 200bp. Libraries were sequenced using Illumina HiSeq 2000. Libraries were generated following Illumina's DNA Sample Prep Kit protocol Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1171655 gds 301171655 GEO Accession GSM1171655 SRX312239 GSM1171656 SRP026218 GSE48176 SRS449828 GSM1171656 ChIP-Seq GENOMIC ChIP Cells were fixed for 10min at RT in 1% formaldehyde, harvested using a cell scraper, washed once in ice-cold PBS, and resuspended in RIPA buffer with protease inhibitor. The sample was then sonicated using an 3.2mm microtip (QSonica Sonicator 4000) at 30s on 30s off intervals and 40% amplitude for 180min while in a -30C 3:1 isopropanol and water bath containing dry ice. Subsequent steps were performed as per the standard protocol. DNA was size-selected during library building to an average fragment size of 200bp. Libraries were sequenced using Illumina HiSeq 2000. Libraries were generated following Illumina's DNA Sample Prep Kit protocol Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1171656 gds 301171656 GEO Accession GSM1171656 SRX312240 GSM1171657 SRP026218 GSE48176 SRS449833 GSM1171657 ChIP-Seq GENOMIC ChIP Cells were fixed for 10min at RT in 1% formaldehyde, harvested using a cell scraper, washed once in ice-cold PBS, and resuspended in RIPA buffer with protease inhibitor. The sample was then sonicated using an 3.2mm microtip (QSonica Sonicator 4000) at 30s on 30s off intervals and 40% amplitude for 180min while in a -30C 3:1 isopropanol and water bath containing dry ice. Subsequent steps were performed as per the standard protocol. DNA was size-selected during library building to an average fragment size of 200bp. Libraries were sequenced using Illumina HiSeq 2000. Libraries were generated following Illumina's DNA Sample Prep Kit protocol Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1171657 gds 301171657 GEO Accession GSM1171657 SRX312241 GSM1171658 SRP026218 GSE48176 SRS449830 GSM1171658 ChIP-Seq GENOMIC ChIP Cells were fixed for 10min at RT in 1% formaldehyde, harvested using a cell scraper, washed once in ice-cold PBS, and resuspended in RIPA buffer with protease inhibitor. The sample was then sonicated using an 3.2mm microtip (QSonica Sonicator 4000) at 30s on 30s off intervals and 40% amplitude for 180min while in a -30C 3:1 isopropanol and water bath containing dry ice. Subsequent steps were performed as per the standard protocol. DNA was size-selected during library building to an average fragment size of 200bp. Libraries were sequenced using Illumina HiSeq 2000. Libraries were generated following Illumina's DNA Sample Prep Kit protocol Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1171658 gds 301171658 GEO Accession GSM1171658 SRX312242 GSM1171659 SRP026218 GSE48176 SRS449831 GSM1171659 ChIP-Seq GENOMIC ChIP Cells were fixed for 10min at RT in 1% formaldehyde, harvested using a cell scraper, washed once in ice-cold PBS, and resuspended in RIPA buffer with protease inhibitor. The sample was then sonicated using an 3.2mm microtip (QSonica Sonicator 4000) at 30s on 30s off intervals and 40% amplitude for 180min while in a -30C 3:1 isopropanol and water bath containing dry ice. Subsequent steps were performed as per the standard protocol. DNA was size-selected during library building to an average fragment size of 200bp. Libraries were sequenced using Illumina HiSeq 2000. Libraries were generated following Illumina's DNA Sample Prep Kit protocol Illumina HiSeq 2000 GEO Sample http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1171659 gds 301171659 GEO Accession GSM1171659