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LOC127897770 H3K27ac hESC enhancer GRCh37_chrX:70584971-70585540 [ Homo sapiens (human) ]

Gene ID: 127897770, updated on 27-Aug-2024

Summary

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Gene symbol
LOC127897770
Gene description
H3K27ac hESC enhancer GRCh37_chrX:70584971-70585540
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 histone modification. [provided by RefSeq, Dec 2022]
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Genomic context

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Location:
chromosome: X
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (71365121..71365690)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (69799223..69799792)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene ZCRB1 pseudogene 1 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:70560484-70561404 Neighboring gene uncharacterized LOC124905198 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29742 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 20897 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 29743 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chrX:70586817-70587512 Neighboring gene RHOG family member 2, pseudogene Neighboring gene TATA-box binding protein associated factor 1 Neighboring gene PABPN1 pseudogene 1 Neighboring gene uncharacterized LOC124905281

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_147123.1 

    Range
    101..670
    Download
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    71365121..71365690
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    69799223..69799792
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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