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LOC126806235 MED14-independent group 3 enhancer GRCh37_chr2:66270681-66271880 [ Homo sapiens (human) ]

Gene ID: 126806235, updated on 10-Oct-2023

Summary

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Gene symbol
LOC126806235
Gene description
MED14-independent group 3 enhancer GRCh37_chr2:66270681-66271880
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. This sequence 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. [provided by RefSeq, Sep 2022]
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Genomic context

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See LOC126806235 in Genome Data Viewer
Location:
chromosome: 2
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (66043547..66044746)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (66054329..66055528)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107985889 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:65927762-65927952 Neighboring gene uncharacterized LOC105369167 Neighboring gene Sharpr-MPRA regulatory region 8914 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:66001201-66001469 Neighboring gene MPRA-validated peak3734 silencer Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:66016952-66017452 Neighboring gene long intergenic non-protein coding RNA 2934 Neighboring gene HHc2:065915 enhancer upstream of MEIS1 Neighboring gene HHc2:065944 enhancer upstream of MEIS1 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr2:66157143-66157642 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr2:66184819-66185607 Neighboring gene VISTA enhancer hs205 Neighboring gene uncharacterized LOC107985890 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr2:66397659-66398858 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:66404589-66405197 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:66470915-66471860 Neighboring gene H3K27ac hESC enhancer GRCh37_chr2:66471861-66472806 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:66475534-66476457 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:66476458-66477380 Neighboring gene uncharacterized LOC107985812

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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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

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_082559.1 

    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    66043547..66044746
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    66054329..66055528
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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