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LOC127396903 NANOG hESC enhancer GRCh37_chr3:20312862-20313363 [ Homo sapiens (human) ]

Gene ID: 127396903, updated on 10-Oct-2023

Summary

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Gene symbol
LOC127396903
Gene description
NANOG hESC enhancer GRCh37_chr3:20312862-20313363
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 naive human embryonic stem cells. This enhancer associates with the NANOG transcription factor. [provided by RefSeq, Oct 2022]
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Genomic context

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Location:
chromosome: 3
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 3 NC_000003.12 (20271370..20271871)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 3 NC_060927.1 (20275364..20275867)

Chromosome 3 - NC_000003.12Genomic Context describing neighboring genes Neighboring gene RNY4 pseudogene 22 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 14136 Neighboring gene MPRA-validated peak4563 silencer Neighboring gene RNA, U6 small nuclear 822, pseudogene Neighboring gene MPRA-validated peak4564 silencer Neighboring gene H3K4me1 hESC enhancer GRCh37_chr3:20353005-20353506 Neighboring gene ReSE screen-validated silencer GRCh37_chr3:20355404-20355578 Neighboring gene uncharacterized LOC101927829 Neighboring gene MPRA-validated peak4565 silencer Neighboring gene MPRA-validated peak4566 silencer Neighboring gene RNA, U6 small nuclear 815, pseudogene

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_098873.1 

    Range
    101..602
    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_000003.12 Reference GRCh38.p14 Primary Assembly

    Range
    20271370..20271871
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060927.1 Alternate T2T-CHM13v2.0

    Range
    20275364..20275867
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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