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LOC116158487 CRISPRi-validated cis-regulatory element chr4.1578 [ Homo sapiens (human) ]

Gene ID: 116158487, updated on 12-Sep-2024

Summary

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Gene symbol
LOC116158487
Gene description
CRISPRi-validated cis-regulatory element chr4.1578
Gene type
biological region
Feature type(s)
regulatory: transcriptional_cis_regulatory_region
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
This genomic region represents a DNase I hypersensitive site (DHS) that was predicted to be an enhancer by the ENCODE (ENCyclopedia Of DNA Elements) project based on various combinations of H3K27 acetylation and binding of p300, GATA1 and RNA polymerase II in K562 erythroleukemia cells. It was validated as a high-confidence cis-regulatory element for the KIT (KIT proto-oncogene, receptor tyrosine kinase) gene on chromosome 4 based on multiplex CRISPR/Cas9-mediated perturbation in K562 cells. [provided by RefSeq, Oct 2019]
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Genomic context

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See LOC116158487 in Genome Data Viewer
Location:
4q
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (54542487..54543098)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (58031292..58031903)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (55408654..55409265)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:55099490-55100040 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21572 Neighboring gene ReSE screen-validated silencer GRCh37_chr4:55100592-55100699 Neighboring gene ReSE screen-validated silencer GRCh37_chr4:55122608-55122834 Neighboring gene platelet derived growth factor receptor alpha Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:55144323-55144846 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr4:55147260-55148459 Neighboring gene ReSE screen-validated silencer GRCh37_chr4:55161059-55161251 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:55191567-55192224 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr4:55190909-55191566 Neighboring gene long intergenic non-protein coding RNA 2283 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:55405507-55406008 Neighboring gene CRISPRi-validated cis-regulatory element chr4.1581 Neighboring gene long intergenic non-protein coding RNA 2260 Neighboring gene Sharpr-MPRA regulatory region 7950 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 21573 Neighboring gene KIT proto-oncogene, receptor tyrosine kinase

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. A Genome-wide Framework for Mapping Gene Regulation via Cellular Genetic Screens. Gasperini M, et al. Cell, 2019 Jan 10. PMID 30612741, Free PMC Article
  2. An integrated encyclopedia of DNA elements in the human genome. ENCODE Project Consortium. Nature, 2012 Sep 6. PMID 22955616, Free PMC Article
  3. The accessible chromatin landscape of the human genome. Thurman RE, et al. Nature, 2012 Sep 6. PMID 22955617, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_066629.1 

    Range
    101..712
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    54542487..54543098
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    58031292..58031903
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    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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