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LOC126807022 CDK7 strongly-dependent group 2 enhancer GRCh37_chr4:31238182-31239381 [ Homo sapiens (human) ]

Gene ID: 126807022, updated on 10-Oct-2023

Summary

Gene symbol
LOC126807022
Gene description
CDK7 strongly-dependent group 2 enhancer GRCh37_chr4:31238182-31239381
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 2 enhancer that depends on the BRD2, BRD4, P300/CBP, MED14 and CDK7 cofactors, with strong dependence on CDK7. [provided by RefSeq, Sep 2022]
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Genomic context

Location:
chromosome: 4
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (31236560..31237759)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (31225229..31226428)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene protocadherin 7 Neighboring gene MT-CYB pseudogene 43 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_78350 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_78356 Neighboring gene NANOG hESC enhancer GRCh37_chr4:31045251-31045820 Neighboring gene long intergenic non-protein coding RNA 2497 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr4:31235626-31236825 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr4:31293032-31293807 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr4:31462532-31463731 Neighboring gene uncharacterized LOC105374564 Neighboring gene long intergenic non-protein coding RNA 2501

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_083343.1 

    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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    31236560..31237759
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    31225229..31226428
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)