SRX832470 GSM1579233 SRP051770 SRS810755 GSM1579233 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579233 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579233 gds 301579233 GEO Accession GSM1579233 SRX832471 GSM1579234 SRP051770 SRS810756 GSM1579234 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579234 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579234 gds 301579234 GEO Accession GSM1579234 SRX832472 GSM1579235 SRP051770 SRS810757 GSM1579235 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579235 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579235 gds 301579235 GEO Accession GSM1579235 SRX832473 GSM1579236 SRP051770 SRS810758 GSM1579236 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579236 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579236 gds 301579236 GEO Accession GSM1579236 SRX832474 GSM1579237 SRP051770 SRS810759 GSM1579237 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579237 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579237 gds 301579237 GEO Accession GSM1579237 SRX832475 GSM1579238 SRP051770 SRS810760 GSM1579238 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579238 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579238 gds 301579238 GEO Accession GSM1579238 SRX832476 GSM1579239 SRP051770 SRS810761 GSM1579239 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579239 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579239 gds 301579239 GEO Accession GSM1579239 SRX832477 GSM1579240 SRP051770 SRS810762 GSM1579240 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579240 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579240 gds 301579240 GEO Accession GSM1579240 SRX832478 GSM1579241 SRP051770 SRS810763 GSM1579241 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579241 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579241 gds 301579241 GEO Accession GSM1579241 SRX832479 GSM1579242 SRP051770 SRS810764 GSM1579242 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579242 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579242 gds 301579242 GEO Accession GSM1579242 SRX832480 GSM1579243 SRP051770 SRS810765 GSM1579243 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579243 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579243 gds 301579243 GEO Accession GSM1579243 SRX832481 GSM1579244 SRP051770 SRS810766 GSM1579244 ChIP-Seq GENOMIC ChIP Crosslinking, extraction and shearing of chromatin was performed by using the Truchip chromatin shearing reagent kit from 300,000 Th2 cells by following manufacturer protocol. Then, sheared chromatin was immunoprecipitated with different antibodies by using the Active Motif's ChIP IT Kit by following manufacturer's instructions Libraries were prepared according to NEB's instructions accompanying the NEBNext Ultra DNA Library Prep Kit for Illumina. After library validation on a fragment analyzer, the purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the MiSeq device following the manufacturer's protocols. Illumina MiSeq GEO Sample GSM1579244 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1579244 gds 301579244 GEO Accession GSM1579244