SRX831872 GSM1577745 SRP051736 PRJNA271704 SRS810184 SAMN03276248 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577745 GSM1577745 GEO Accession GSM1577745 SRX831873 GSM1577746 SRP051736 PRJNA271704 SRS810185 SAMN03276247 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577746 GSM1577746 GEO Accession GSM1577746 SRX831874 GSM1577747 SRP051736 PRJNA271704 SRS810186 SAMN03276381 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577747 GSM1577747 GEO Accession GSM1577747 SRX831875 GSM1577748 SRP051736 PRJNA271704 SRS810188 SAMN03276379 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577748 GSM1577748 GEO Accession GSM1577748 SRX831876 GSM1577749 SRP051736 PRJNA271704 SRS810187 SAMN03276389 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577749 GSM1577749 GEO Accession GSM1577749 SRX831877 GSM1577750 SRP051736 PRJNA271704 SRS810189 SAMN03276390 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577750 GSM1577750 GEO Accession GSM1577750 SRX831878 GSM1577751 SRP051736 PRJNA271704 SRS810191 SAMN03276383 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577751 GSM1577751 GEO Accession GSM1577751 SRX831879 GSM1577752 SRP051736 PRJNA271704 SRS810190 SAMN03276382 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577752 GSM1577752 GEO Accession GSM1577752 SRX831880 GSM1577753 SRP051736 PRJNA271704 SRS810192 SAMN03276388 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577753 GSM1577753 GEO Accession GSM1577753 SRX831881 GSM1577754 SRP051736 PRJNA271704 SRS810193 SAMN03276385 ChIP-Seq GENOMIC ChIP For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577754 GSM1577754 GEO Accession GSM1577754 SRX831882 GSM1577755 SRP051736 PRJNA271704 SRS810194 SAMN03276386 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577755 GSM1577755 GEO Accession GSM1577755 SRX831883 GSM1577756 SRP051736 PRJNA271704 SRS810195 SAMN03276384 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577756 GSM1577756 GEO Accession GSM1577756 SRX831884 GSM1577757 SRP051736 PRJNA271704 SRS810196 SAMN03276380 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577757 GSM1577757 GEO Accession GSM1577757 SRX831885 GSM1577758 SRP051736 PRJNA271704 SRS810197 SAMN03276387 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577758 GSM1577758 GEO Accession GSM1577758 SRX831886 GSM1577759 SRP051736 PRJNA271704 SRS810199 SAMN03276394 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577759 GSM1577759 GEO Accession GSM1577759 SRX831887 GSM1577760 SRP051736 PRJNA271704 SRS810198 SAMN03276391 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577760 GSM1577760 GEO Accession GSM1577760 SRX831888 GSM1577761 SRP051736 PRJNA271704 SRS810200 SAMN03276396 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577761 GSM1577761 GEO Accession GSM1577761 SRX831889 GSM1577762 SRP051736 PRJNA271704 SRS810201 SAMN03276392 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577762 GSM1577762 GEO Accession GSM1577762 SRX831890 GSM1577763 SRP051736 PRJNA271704 SRS810204 SAMN03276395 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577763 GSM1577763 GEO Accession GSM1577763 SRX831891 GSM1577764 SRP051736 PRJNA271704 SRS810203 SAMN03276393 RNA-Seq TRANSCRIPTOMIC cDNA For RNA-Seq, RNA from 5 donors was pooled, and 1 μg of the pooled RNA was used to synthesize cDNA 220-400 bp fragments were isolated using 2% E-Gel (Invitrogen), ends were repaired, adaptor was added using T4 DNA ligase (New England Biolabs), and amplified for 17 cycles using PE 1.0 and PE 2.0 primers (Illumina) and Phusion High Fidelity PCR Master Mix (New England Biolabs). For ChIP-Seq, Chromatin from 10-20 million cells was sonicated into 250-500 bp fragments, DNA ends were repaired using polynucleotide kinase and Klenow enzyme, and treated with Taq polymerase to generate a protruding 3' “A” nucleotide. DNA fragments of ~250-450 bp were purified from agarose gels and used for cluster generation and sequencing. Antibody against STAT5B was used for immunoprecipitation. PCR products were barcoded (indexed) and sequenced on Illumina HiSeq 2000 platform. Illumina HiSeq 2000 gds 301577764 GSM1577764 GEO Accession GSM1577764