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Gene : 108281173 Homo sapiens

Description  This genomic element is located in the intergenic region between the ZNF619P1 (zinc finger protein 619 pseudogene 1) and HMGN1P19 (high mobility group nucleosome binding domain 1 pseudogene 19) loci. It was defined as a nontranscribed region with regulatory potential based on the co-occurrence of H3K27ac and H3K4me1 ChIP-seq data centered on P300 binding sites in HeLa cells, with an absence of capped transcripts by cap analysis of gene expression (CAGE). It was validated as a functional enhancer by reporter assays in HeLa cells. [provided by RefSeq, Jul 2016]
  • identifiers:
  • 108281173

Genome feature

Region: gene ?
Location: No location information in HumanMine


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Function

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0 Pathways

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

0 Pathways

0 SN Ps

0 Cross References

1 Data Sets

0 Homologues

0 Located Features

0 Rna Seq Results