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    LOC126863190 BRD4-independent group 4 enhancer GRCh37_chrX:3445471-3446670 [ Homo sapiens (human) ]

    Gene ID: 126863190, updated on 10-Oct-2023

    Summary

    Gene symbol
    LOC126863190
    Gene description
    BRD4-independent group 4 enhancer GRCh37_chrX:3445471-3446670
    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 4 enhancer that depends on the BRD2, P300/CBP, MED14 and CDK7 cofactors, but it has limited or no dependence on the BRD4 bromodomain protein. [provided by RefSeq, Sep 2022]
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    Genomic context

    Location:
    chromosome: X
    Annotation release Status Assembly Chr Location
    RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (3527430..3528629)
    RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (3141631..3142830)

    Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene matrix remodeling associated 5 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chrX:3280933-3281483 Neighboring gene argininosuccinate synthetase 1 pseudogene 4 Neighboring gene small nucleolar RNA, H/ACA box 48B Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chrX:3470673-3471624 Neighboring gene RNA, U6 small nuclear 114, pseudogene

    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_087686.1 

      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_000023.11 Reference GRCh38.p14 Primary Assembly

      Range
      3527430..3528629
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060947.1 Alternate T2T-CHM13v2.0

      Range
      3141631..3142830
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)