SRX382119 GSM1273545 SRP033270 GSE52648 SRS506334 GSM1273545 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibody. 28 ug of sonicated chromatin was used for the Grhl3 IPs. Sequencing libraries were generated for the Grhl3 and Input samples using Illumina Tru-Seq ChIP-Seq kit, multiplexed to be sequenced in a single lane, according to the Illumina protocol for ChIP-Seq library preparation, with some modification. After adaptor ligation, PCR amplification was performed prior to size selection of the library [Schmidt D, Methods, 2009]. Clustering and 50-cycle single end sequencing were performed on the Illumina Hi-Seq 2000 Genome Analyzer. Illumina HiSeq 2000 GEO Sample GSM1273545 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1273545 gds 301273545 GEO Accession GSM1273545 SRX382120 GSM1273546 SRP033270 GSE52648 SRS506335 GSM1273546 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibody. 28 ug of sonicated chromatin was used for the Grhl3 IPs. Sequencing libraries were generated for the Grhl3 and Input samples using Illumina Tru-Seq ChIP-Seq kit, multiplexed to be sequenced in a single lane, according to the Illumina protocol for ChIP-Seq library preparation, with some modification. After adaptor ligation, PCR amplification was performed prior to size selection of the library [Schmidt D, Methods, 2009]. Clustering and 50-cycle single end sequencing were performed on the Illumina Hi-Seq 2000 Genome Analyzer. Illumina HiSeq 2000 GEO Sample GSM1273546 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1273546 gds 301273546 GEO Accession GSM1273546 SRX382121 GSM1273547 SRP033270 GSE52648 SRS506336 GSM1273547 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibody. 28 ug of sonicated chromatin was used for the Grhl3 IPs. Sequencing libraries were generated for the Grhl3 and Input samples using Illumina Tru-Seq ChIP-Seq kit, multiplexed to be sequenced in a single lane, according to the Illumina protocol for ChIP-Seq library preparation, with some modification. After adaptor ligation, PCR amplification was performed prior to size selection of the library [Schmidt D, Methods, 2009]. Clustering and 50-cycle single end sequencing were performed on the Illumina Hi-Seq 2000 Genome Analyzer. Illumina HiSeq 2000 GEO Sample GSM1273547 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1273547 gds 301273547 GEO Accession GSM1273547 SRX382122 GSM1273548 SRP033270 GSE52648 SRS506337 GSM1273548 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibody. 28 ug of sonicated chromatin was used for the Grhl3 IPs. Sequencing libraries were generated for the Grhl3 and Input samples using Illumina Tru-Seq ChIP-Seq kit, multiplexed to be sequenced in a single lane, according to the Illumina protocol for ChIP-Seq library preparation, with some modification. After adaptor ligation, PCR amplification was performed prior to size selection of the library [Schmidt D, Methods, 2009]. Clustering and 50-cycle single end sequencing were performed on the Illumina Hi-Seq 2000 Genome Analyzer. Illumina HiSeq 2000 GEO Sample GSM1273548 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1273548 gds 301273548 GEO Accession GSM1273548 SRX382123 GSM1273549 SRP033270 GSE52648 SRS506338 GSM1273549 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibody. 28 ug of sonicated chromatin was used for the Grhl3 IPs. Sequencing libraries were generated for the Grhl3 and Input samples using Illumina Tru-Seq ChIP-Seq kit, multiplexed to be sequenced in a single lane, according to the Illumina protocol for ChIP-Seq library preparation, with some modification. After adaptor ligation, PCR amplification was performed prior to size selection of the library [Schmidt D, Methods, 2009]. Clustering and 50-cycle single end sequencing were performed on the Illumina Hi-Seq 2000 Genome Analyzer. Illumina HiSeq 2000 GEO Sample GSM1273549 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1273549 gds 301273549 GEO Accession GSM1273549 SRX382124 GSM1273550 SRP033270 GSE52648 SRS506339 GSM1273550 ChIP-Seq GENOMIC ChIP Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibody. 28 ug of sonicated chromatin was used for the Grhl3 IPs. Sequencing libraries were generated for the Grhl3 and Input samples using Illumina Tru-Seq ChIP-Seq kit, multiplexed to be sequenced in a single lane, according to the Illumina protocol for ChIP-Seq library preparation, with some modification. After adaptor ligation, PCR amplification was performed prior to size selection of the library [Schmidt D, Methods, 2009]. Clustering and 50-cycle single end sequencing were performed on the Illumina Hi-Seq 2000 Genome Analyzer. Illumina HiSeq 2000 GEO Sample GSM1273550 http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1273550 gds 301273550 GEO Accession GSM1273550