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LOC127408042 H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:220337-221331 [ Homo sapiens (human) ]

Gene ID: 127408042, updated on 10-Oct-2023

Summary

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Gene symbol
LOC127408042
Gene description
H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:220337-221331
Gene type
biological region
Feature type(s)
regulatory: enhancer
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 was validated as an active enhancer by the ChIP-STARR-seq massively parallel reporter assay in primed human embryonic stem cells. This enhancer is marked by the H3K27ac and H3K4me1 histone modifications. [provided by RefSeq, Oct 2022]
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Genomic context

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Location:
chromosome: 7
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 7 NC_000007.14 (220337..221331)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 7 NC_060931.1 (322183..323179)

Chromosome 7 - NC_000007.14Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124901806 Neighboring gene uncharacterized LOC124901808 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:188255-188923 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:195348-196325 Neighboring gene ReSE screen-validated silencer GRCh37_chr7:200334-200504 Neighboring gene FAM20C golgi associated secretory pathway kinase Neighboring gene ReSE screen-validated silencer GRCh37_chr7:205256-205424 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:206083-206732 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:206733-207382 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:214209-214786 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:218347-219342 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr7:221332-222325 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr7:226080-226580 Neighboring gene G patch domain-containing protein 8-like Neighboring gene FOXL3 overlapping transcript 1 Neighboring gene forkhead box L3

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. Functional Dissection of the Enhancer Repertoire in Human Embryonic Stem Cells. Barakat TS, et al. Cell Stem Cell, 2018 Aug 2. PMID 30033119, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

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_110010.1 

    Range
    101..1095
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000007.14 Reference GRCh38.p14 Primary Assembly

    Range
    220337..221331
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    GenBank, FASTA, Sequence Viewer (Graphics)

Reference GRCh38.p14 PATCHES

Genomic

  1. NW_021159998.1 Reference GRCh38.p14 PATCHES

    Range
    196025..197019
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060931.1 Alternate T2T-CHM13v2.0

    Range
    322183..323179
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    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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