SRX3777688 GSM3032542 SRP134244 SRS3031577 GSM3032542 OTHER GENOMIC other Cultured cells and liver tissue were crosslinked in 1 % formaldehyde for 15 minutes. A 5 minute quench was performed with 125mM glycine. To prepare ChIP extracts, nuclei were prepared by hypotonic lysis followed by Dounce homogenization. Nuclei were resuspended in SDS lysis buffer (50 mM HEPES/NaOH pH 7.5, 1% SDS, 10 mM EDTA, Complete protease inhibitor), incubated at 4 C for 10 min, and subjected to microtip probe sonication under conditions optimized for IP efficiency. ChIP-Seq libraries were produced and sequenced according to Illumina protocols. Libraries were multiplexed for sequencing. Illumina HiSeq 2000 gds 303032542 GSM3032542 GEO Accession GSM3032542 SRX3777689 GSM3032543 SRP134244 SRS3031578 GSM3032543 OTHER GENOMIC other Cultured cells and liver tissue were crosslinked in 1 % formaldehyde for 15 minutes. A 5 minute quench was performed with 125mM glycine. To prepare ChIP extracts, nuclei were prepared by hypotonic lysis followed by Dounce homogenization. Nuclei were resuspended in SDS lysis buffer (50 mM HEPES/NaOH pH 7.5, 1% SDS, 10 mM EDTA, Complete protease inhibitor), incubated at 4 C for 10 min, and subjected to microtip probe sonication under conditions optimized for IP efficiency. ChIP-Seq libraries were produced and sequenced according to Illumina protocols. Libraries were multiplexed for sequencing. Illumina HiSeq 2000 gds 303032543 GSM3032543 GEO Accession GSM3032543 SRX3777690 GSM3032544 SRP134244 SRS3031579 GSM3032544 OTHER GENOMIC other Cultured cells and liver tissue were crosslinked in 1 % formaldehyde for 15 minutes. A 5 minute quench was performed with 125mM glycine. To prepare ChIP extracts, nuclei were prepared by hypotonic lysis followed by Dounce homogenization. Nuclei were resuspended in SDS lysis buffer (50 mM HEPES/NaOH pH 7.5, 1% SDS, 10 mM EDTA, Complete protease inhibitor), incubated at 4 C for 10 min, and subjected to microtip probe sonication under conditions optimized for IP efficiency. ChIP-Seq libraries were produced and sequenced according to Illumina protocols. Libraries were multiplexed for sequencing. Illumina HiSeq 2000 gds 303032544 GSM3032544 GEO Accession GSM3032544 SRX3777691 GSM3032545 SRP134244 SRS3031581 GSM3032545 OTHER GENOMIC other Cultured cells and liver tissue were crosslinked in 1 % formaldehyde for 15 minutes. A 5 minute quench was performed with 125mM glycine. To prepare ChIP extracts, nuclei were prepared by hypotonic lysis followed by Dounce homogenization. Nuclei were resuspended in SDS lysis buffer (50 mM HEPES/NaOH pH 7.5, 1% SDS, 10 mM EDTA, Complete protease inhibitor), incubated at 4 C for 10 min, and subjected to microtip probe sonication under conditions optimized for IP efficiency. ChIP-Seq libraries were produced and sequenced according to Illumina protocols. Libraries were multiplexed for sequencing. Illumina HiSeq 2000 gds 303032545 GSM3032545 GEO Accession GSM3032545 SRX3777692 GSM3032546 SRP134244 SRS3031580 GSM3032546 OTHER GENOMIC other Cultured cells and liver tissue were crosslinked in 1 % formaldehyde for 15 minutes. A 5 minute quench was performed with 125mM glycine. To prepare ChIP extracts, nuclei were prepared by hypotonic lysis followed by Dounce homogenization. Nuclei were resuspended in SDS lysis buffer (50 mM HEPES/NaOH pH 7.5, 1% SDS, 10 mM EDTA, Complete protease inhibitor), incubated at 4 C for 10 min, and subjected to microtip probe sonication under conditions optimized for IP efficiency. ChIP-Seq libraries were produced and sequenced according to Illumina protocols. Libraries were multiplexed for sequencing. Illumina HiSeq 2000 gds 303032546 GSM3032546 GEO Accession GSM3032546 SRX3777693 GSM3032547 SRP134244 SRS3031582 GSM3032547 OTHER GENOMIC other Cultured cells and liver tissue were crosslinked in 1 % formaldehyde for 15 minutes. A 5 minute quench was performed with 125mM glycine. To prepare ChIP extracts, nuclei were prepared by hypotonic lysis followed by Dounce homogenization. Nuclei were resuspended in SDS lysis buffer (50 mM HEPES/NaOH pH 7.5, 1% SDS, 10 mM EDTA, Complete protease inhibitor), incubated at 4 C for 10 min, and subjected to microtip probe sonication under conditions optimized for IP efficiency. ChIP-Seq libraries were produced and sequenced according to Illumina protocols. Libraries were multiplexed for sequencing. Illumina HiSeq 2000 gds 303032547 GSM3032547 GEO Accession GSM3032547 SRX3777694 GSM3032548 SRP134244 SRS3031583 GSM3032548 OTHER GENOMIC other Cultured cells and liver tissue were crosslinked in 1 % formaldehyde for 15 minutes. A 5 minute quench was performed with 125mM glycine. To prepare ChIP extracts, nuclei were prepared by hypotonic lysis followed by Dounce homogenization. Nuclei were resuspended in SDS lysis buffer (50 mM HEPES/NaOH pH 7.5, 1% SDS, 10 mM EDTA, Complete protease inhibitor), incubated at 4 C for 10 min, and subjected to microtip probe sonication under conditions optimized for IP efficiency. ChIP-Seq libraries were produced and sequenced according to Illumina protocols. Libraries were multiplexed for sequencing. Illumina HiSeq 2000 gds 303032548 GSM3032548 GEO Accession GSM3032548 SRX3777695 GSM3032549 SRP134244 SRS3031585 GSM3032549 OTHER GENOMIC other Cultured cells and liver tissue were crosslinked in 1 % formaldehyde for 15 minutes. A 5 minute quench was performed with 125mM glycine. To prepare ChIP extracts, nuclei were prepared by hypotonic lysis followed by Dounce homogenization. Nuclei were resuspended in SDS lysis buffer (50 mM HEPES/NaOH pH 7.5, 1% SDS, 10 mM EDTA, Complete protease inhibitor), incubated at 4 C for 10 min, and subjected to microtip probe sonication under conditions optimized for IP efficiency. ChIP-Seq libraries were produced and sequenced according to Illumina protocols. Libraries were multiplexed for sequencing. Illumina HiSeq 2000 gds 303032549 GSM3032549 GEO Accession GSM3032549 SRX3777696 GSM3032550 SRP134244 SRS3031584 GSM3032550 OTHER GENOMIC other Cultured cells and liver tissue were crosslinked in 1 % formaldehyde for 15 minutes. A 5 minute quench was performed with 125mM glycine. To prepare ChIP extracts, nuclei were prepared by hypotonic lysis followed by Dounce homogenization. Nuclei were resuspended in SDS lysis buffer (50 mM HEPES/NaOH pH 7.5, 1% SDS, 10 mM EDTA, Complete protease inhibitor), incubated at 4 C for 10 min, and subjected to microtip probe sonication under conditions optimized for IP efficiency. ChIP-Seq libraries were produced and sequenced according to Illumina protocols. Libraries were multiplexed for sequencing. Illumina HiSeq 2000 gds 303032550 GSM3032550 GEO Accession GSM3032550