SRX12740000 GSM5651365 SRP342719 SRS10688244 GSM5651365 ChIP-Seq GENOMIC ChIP Cells were crosslinked and immunoprecipitated with HA antibody (ab9110) as described in Wilbanks et al 2012 (doi: 10.1093/nar/gks063) with the following changes to the protocol: the cross-linking reaction was allowed to proceed for 20 minutes rather than 10, and cell pellets were resupended in 800 μL lysis buffer instead of 1.6mL. Libraries were constructed using the KAPA Hyper Prep kit and Illumina TruSeq adapters according to manufactuer's instructions. DNA library quality was assessed by Bioanalyzer using a High Sensitivity DNA chip (Agilent) . Samples were pooled and run on an Illumina NovaSeq 6000 (Duke Sequencing and Genomics Technologies core) for paired-end sequencing. Illumina NovaSeq 6000 gds 305651365 GSM5651365 GEO Accession GSM5651365 SRX12740001 GSM5651366 SRP342719 SRS10688245 GSM5651366 ChIP-Seq GENOMIC ChIP Cells were crosslinked and immunoprecipitated with HA antibody (ab9110) as described in Wilbanks et al 2012 (doi: 10.1093/nar/gks063) with the following changes to the protocol: the cross-linking reaction was allowed to proceed for 20 minutes rather than 10, and cell pellets were resupended in 800 μL lysis buffer instead of 1.6mL. Libraries were constructed using the KAPA Hyper Prep kit and Illumina TruSeq adapters according to manufactuer's instructions. DNA library quality was assessed by Bioanalyzer using a High Sensitivity DNA chip (Agilent) . Samples were pooled and run on an Illumina NovaSeq 6000 (Duke Sequencing and Genomics Technologies core) for paired-end sequencing. Illumina NovaSeq 6000 gds 305651366 GSM5651366 GEO Accession GSM5651366 SRX12740002 GSM5651367 SRP342719 SRS10688246 GSM5651367 ChIP-Seq GENOMIC ChIP Cells were crosslinked and immunoprecipitated with HA antibody (ab9110) as described in Wilbanks et al 2012 (doi: 10.1093/nar/gks063) with the following changes to the protocol: the cross-linking reaction was allowed to proceed for 20 minutes rather than 10, and cell pellets were resupended in 800 μL lysis buffer instead of 1.6mL. Libraries were constructed using the KAPA Hyper Prep kit and Illumina TruSeq adapters according to manufactuer's instructions. DNA library quality was assessed by Bioanalyzer using a High Sensitivity DNA chip (Agilent) . Samples were pooled and run on an Illumina NovaSeq 6000 (Duke Sequencing and Genomics Technologies core) for paired-end sequencing. Illumina NovaSeq 6000 gds 305651367 GSM5651367 GEO Accession GSM5651367 SRX12740003 GSM5651368 SRP342719 SRS10688247 GSM5651368 ChIP-Seq GENOMIC ChIP Cells were crosslinked and immunoprecipitated with HA antibody (ab9110) as described in Wilbanks et al 2012 (doi: 10.1093/nar/gks063) with the following changes to the protocol: the cross-linking reaction was allowed to proceed for 20 minutes rather than 10, and cell pellets were resupended in 800 μL lysis buffer instead of 1.6mL. Libraries were constructed using the KAPA Hyper Prep kit and Illumina TruSeq adapters according to manufactuer's instructions. DNA library quality was assessed by Bioanalyzer using a High Sensitivity DNA chip (Agilent) . Samples were pooled and run on an Illumina NovaSeq 6000 (Duke Sequencing and Genomics Technologies core) for paired-end sequencing. Illumina NovaSeq 6000 gds 305651368 GSM5651368 GEO Accession GSM5651368 SRX12740004 GSM5651369 SRP342719 SRS10688248 GSM5651369 ChIP-Seq GENOMIC ChIP Cells were crosslinked and immunoprecipitated with HA antibody (ab9110) as described in Wilbanks et al 2012 (doi: 10.1093/nar/gks063) with the following changes to the protocol: the cross-linking reaction was allowed to proceed for 20 minutes rather than 10, and cell pellets were resupended in 800 μL lysis buffer instead of 1.6mL. Libraries were constructed using the KAPA Hyper Prep kit and Illumina TruSeq adapters according to manufactuer's instructions. DNA library quality was assessed by Bioanalyzer using a High Sensitivity DNA chip (Agilent) . Samples were pooled and run on an Illumina NovaSeq 6000 (Duke Sequencing and Genomics Technologies core) for paired-end sequencing. Illumina NovaSeq 6000 gds 305651369 GSM5651369 GEO Accession GSM5651369 SRX12740005 GSM5651370 SRP342719 SRS10688249 GSM5651370 ChIP-Seq GENOMIC ChIP Cells were crosslinked and immunoprecipitated with HA antibody (ab9110) as described in Wilbanks et al 2012 (doi: 10.1093/nar/gks063) with the following changes to the protocol: the cross-linking reaction was allowed to proceed for 20 minutes rather than 10, and cell pellets were resupended in 800 μL lysis buffer instead of 1.6mL. Libraries were constructed using the KAPA Hyper Prep kit and Illumina TruSeq adapters according to manufactuer's instructions. DNA library quality was assessed by Bioanalyzer using a High Sensitivity DNA chip (Agilent) . Samples were pooled and run on an Illumina NovaSeq 6000 (Duke Sequencing and Genomics Technologies core) for paired-end sequencing. Illumina NovaSeq 6000 gds 305651370 GSM5651370 GEO Accession GSM5651370 SRX12740006 GSM5651371 SRP342719 SRS10688250 GSM5651371 ChIP-Seq GENOMIC ChIP Cells were crosslinked and immunoprecipitated with HA antibody (ab9110) as described in Wilbanks et al 2012 (doi: 10.1093/nar/gks063) with the following changes to the protocol: the cross-linking reaction was allowed to proceed for 20 minutes rather than 10, and cell pellets were resupended in 800 μL lysis buffer instead of 1.6mL. Libraries were constructed using the KAPA Hyper Prep kit and Illumina TruSeq adapters according to manufactuer's instructions. DNA library quality was assessed by Bioanalyzer using a High Sensitivity DNA chip (Agilent) . Samples were pooled and run on an Illumina NovaSeq 6000 (Duke Sequencing and Genomics Technologies core) for paired-end sequencing. Illumina NovaSeq 6000 gds 305651371 GSM5651371 GEO Accession GSM5651371 SRX12740007 GSM5651372 SRP342719 SRS10688251 GSM5651372 ChIP-Seq GENOMIC ChIP Cells were crosslinked and immunoprecipitated with HA antibody (ab9110) as described in Wilbanks et al 2012 (doi: 10.1093/nar/gks063) with the following changes to the protocol: the cross-linking reaction was allowed to proceed for 20 minutes rather than 10, and cell pellets were resupended in 800 μL lysis buffer instead of 1.6mL. Libraries were constructed using the KAPA Hyper Prep kit and Illumina TruSeq adapters according to manufactuer's instructions. DNA library quality was assessed by Bioanalyzer using a High Sensitivity DNA chip (Agilent) . Samples were pooled and run on an Illumina NovaSeq 6000 (Duke Sequencing and Genomics Technologies core) for paired-end sequencing. Illumina NovaSeq 6000 gds 305651372 GSM5651372 GEO Accession GSM5651372