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LOC126860985 MED14-independent group 3 enhancer GRCh37_chr10:85743139-85744338 [ Homo sapiens (human) ]

Gene ID: 126860985, updated on 10-Oct-2023

Summary

Gene symbol
LOC126860985
Gene description
MED14-independent group 3 enhancer GRCh37_chr10:85743139-85744338
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

Location:
chromosome: 10
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (83983383..83984582)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (84861545..84862744)

Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC107984181 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr10:85691876-85692426 Neighboring gene uncharacterized LOC105378398 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr10:85716832-85717790 Neighboring gene uncharacterized LOC105378399 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 3673 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_17591 Neighboring gene RNA, U1 small nuclear 65, pseudogene Neighboring gene high mobility group nucleosomal binding domain 2 pseudogene 8

Genomic regions, transcripts, and products

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_085484.1 

    Range
    101..1300
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    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_000010.11 Reference GRCh38.p14 Primary Assembly

    Range
    83983383..83984582
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060934.1 Alternate T2T-CHM13v2.0

    Range
    84861545..84862744
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    GenBank, FASTA, Sequence Viewer (Graphics)