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LOC126805779 MED14-independent group 3 enhancer GRCh37_chr1:88500769-88501968 [ Homo sapiens (human) ]

Gene ID: 126805779, updated on 10-Oct-2023

Summary

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Gene symbol
LOC126805779
Gene description
MED14-independent group 3 enhancer GRCh37_chr1:88500769-88501968
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 STARR-seq (self-transcribing active regulatory region sequencing) massively parallel reporter assay in HCT116 colorectal carcinoma cells, where it was defined as a group 3 enhancer that depends on the BRD2, BRD4, P300/CBP and CDK7 cofactors, but it has limited or no dependence on the MED14 core Mediator complex subunit. A subregion was also validated as an enhancer by ChIP-STARR-seq in primed human embryonic stem cells, where it is marked by the H3K27ac and H3K4me1 histone modifications. [provided by RefSeq, Dec 2022]
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Genomic context

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See LOC126805779 in Genome Data Viewer
Location:
chromosome: 1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (88035086..88036285)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (87878317..87879516)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1773 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr1:88406737-88407433 Neighboring gene uncharacterized LOC101927871 Neighboring gene uncharacterized LOC105378836 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:88433977-88434478 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:88434479-88434978 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr1:88439514-88440031 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:88503107-88503807 Neighboring gene VISTA enhancer hs1198 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:88553815-88554316 Neighboring gene VISTA enhancer hs878 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:88641175-88642374 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1050 Neighboring gene VISTA enhancer hs1107 Neighboring gene NANOG hESC enhancer GRCh37_chr1:88761804-88762778 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:88807244-88807797 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1289 Neighboring gene VISTA enhancer hs327 Neighboring gene uncharacterized LOC105378839 Neighboring gene RNA, 7SL, cytoplasmic 583, 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. Differential cofactor dependencies define distinct types of human enhancers. Neumayr C, et al. Nature, 2022 Jun. PMID 35650434, Free PMC Article
  2. 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

Variation

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See variants in ClinVar

General gene information

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Other Names

  • H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:88501001-88501702

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_082103.1 

    Range
    101..1300
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    88035086..88036285
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    87878317..87879516
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    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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