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H3K27ac, H3K4me and H3K4me3 binding examined by ChIP-seq in the CHP-134 neuroblastoma cell line

ABSTRACT: H3K27ac, H3K4me and H3K4me3 binding examined by ChIP-seq in the CHP-134 neuroblastoma cell line

PROVIDER: PRJNA450134 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR7002020.fastq.gz	Fastqsanger.gz
	SRR7002021.fastq.gz	Fastqsanger.gz
	SRR7002022.fastq.gz	Fastqsanger.gz
	SRR7002023.fastq.gz	Fastqsanger.gz
	SRR7002024.fastq.gz	Fastqsanger.gz

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H3K27ac, H3K4me and H3K4me3 binding examined by ChIP-seq in the CHP-134 neuroblastoma cell line

Project description:Super-enhancers are defined by peaks in H3K27 acetylation and H3K4 mono-methylation, and the lack of H3K4 tri-methylation. They have been found to play a role in oncogene transcription and tumour maintenance. Using ChIP-Seq, we profiled H3K27ac, H3K4me and H3K4me3 binding in CHP-134 neuroblastoma cells. We identified H3K27ac, H3K4me and H3K4me3 binding sites in the CHP-134 neuroblastoma cell line.

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