SRX2498433 GSM2460995 SRP096899 SRS1925286 GSM2460995 ChIP-Seq GENOMIC ChIP In general, Flag ChIP followed the procedure described in Frank et al., 2001. Chromatin was fixed on 1% formaldehyde for 10 minutes and was sonicated on a bioruptor (Diagenode) to produce fragments of 100-500 bp. 500 μg of protein were used per ChIP with 10 μg of anti-Flag antibody (Sigma, catalog number F1804) and protein-bound fragments were retrieved with ProteinG-coupled magnetic Dynabeads (Invitrogen). Sequencing libraries were prepared using the NEBNext® UltraTM DNA Library Prep Kit and Multiplex Oligos (New England Biolabs) from 5 ng of DNA. Illumina HiSeq 2000 gds 302460995 GEO Accession GSM2460995 SRX2498434 GSM2460996 SRP096899 SRS1925285 GSM2460996 ChIP-Seq GENOMIC ChIP In general, Flag ChIP followed the procedure described in Frank et al., 2001. Chromatin was fixed on 1% formaldehyde for 10 minutes and was sonicated on a bioruptor (Diagenode) to produce fragments of 100-500 bp. 500 μg of protein were used per ChIP with 10 μg of anti-Flag antibody (Sigma, catalog number F1804) and protein-bound fragments were retrieved with ProteinG-coupled magnetic Dynabeads (Invitrogen). Sequencing libraries were prepared using the NEBNext® UltraTM DNA Library Prep Kit and Multiplex Oligos (New England Biolabs) from 5 ng of DNA. Illumina HiSeq 2000 gds 302460996 GEO Accession GSM2460996 SRX2498435 GSM2460997 SRP096899 SRS1925287 GSM2460997 ChIP-Seq GENOMIC ChIP In general, Flag ChIP followed the procedure described in Frank et al., 2001. Chromatin was fixed on 1% formaldehyde for 10 minutes and was sonicated on a bioruptor (Diagenode) to produce fragments of 100-500 bp. 500 μg of protein were used per ChIP with 10 μg of anti-Flag antibody (Sigma, catalog number F1804) and protein-bound fragments were retrieved with ProteinG-coupled magnetic Dynabeads (Invitrogen). Sequencing libraries were prepared using the NEBNext® UltraTM DNA Library Prep Kit and Multiplex Oligos (New England Biolabs) from 5 ng of DNA. Illumina HiSeq 2000 gds 302460997 GEO Accession GSM2460997 SRX2498436 GSM2460998 SRP096899 SRS1925288 GSM2460998 ChIP-Seq GENOMIC ChIP In general, Flag ChIP followed the procedure described in Frank et al., 2001. Chromatin was fixed on 1% formaldehyde for 10 minutes and was sonicated on a bioruptor (Diagenode) to produce fragments of 100-500 bp. 500 μg of protein were used per ChIP with 10 μg of anti-Flag antibody (Sigma, catalog number F1804) and protein-bound fragments were retrieved with ProteinG-coupled magnetic Dynabeads (Invitrogen). Sequencing libraries were prepared using the NEBNext® UltraTM DNA Library Prep Kit and Multiplex Oligos (New England Biolabs) from 5 ng of DNA. Illumina HiSeq 2000 gds 302460998 GEO Accession GSM2460998 SRX2498437 GSM2460999 SRP096899 SRS1925289 GSM2460999 ChIP-Seq GENOMIC ChIP In general, Flag ChIP followed the procedure described in Frank et al., 2001. Chromatin was fixed on 1% formaldehyde for 10 minutes and was sonicated on a bioruptor (Diagenode) to produce fragments of 100-500 bp. 500 μg of protein were used per ChIP with 10 μg of anti-Flag antibody (Sigma, catalog number F1804) and protein-bound fragments were retrieved with ProteinG-coupled magnetic Dynabeads (Invitrogen). Sequencing libraries were prepared using the NEBNext® UltraTM DNA Library Prep Kit and Multiplex Oligos (New England Biolabs) from 5 ng of DNA. Illumina HiSeq 2000 gds 302460999 GEO Accession GSM2460999 SRX2498438 GSM2461000 SRP096899 SRS1925290 GSM2461000 ChIP-Seq GENOMIC ChIP In general, Flag ChIP followed the procedure described in Frank et al., 2001. Chromatin was fixed on 1% formaldehyde for 10 minutes and was sonicated on a bioruptor (Diagenode) to produce fragments of 100-500 bp. 500 μg of protein were used per ChIP with 10 μg of anti-Flag antibody (Sigma, catalog number F1804) and protein-bound fragments were retrieved with ProteinG-coupled magnetic Dynabeads (Invitrogen). Sequencing libraries were prepared using the NEBNext® UltraTM DNA Library Prep Kit and Multiplex Oligos (New England Biolabs) from 5 ng of DNA. Illumina HiSeq 2000 gds 302461000 GEO Accession GSM2461000 SRX2498439 GSM2461001 SRP096899 SRS1925291 GSM2461001 ChIP-Seq GENOMIC ChIP In general, Flag ChIP followed the procedure described in Frank et al., 2001. Chromatin was fixed on 1% formaldehyde for 10 minutes and was sonicated on a bioruptor (Diagenode) to produce fragments of 100-500 bp. 500 μg of protein were used per ChIP with 10 μg of anti-Flag antibody (Sigma, catalog number F1804) and protein-bound fragments were retrieved with ProteinG-coupled magnetic Dynabeads (Invitrogen). Sequencing libraries were prepared using the NEBNext® UltraTM DNA Library Prep Kit and Multiplex Oligos (New England Biolabs) from 5 ng of DNA. Illumina HiSeq 2000 gds 302461001 GEO Accession GSM2461001