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LOC126861912 CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:32370891-32372090 [ Homo sapiens (human) ]

Gene ID: 126861912, updated on 10-Oct-2023

Summary

Gene symbol
LOC126861912
Gene description
CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:32370891-32372090
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

See LOC126861912 in Genome Data Viewer
Location:
chromosome: 14
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (31901685..31902884)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (26098999..26100198)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene NUBP iron-sulfur cluster assembly factor, mitochondrial Neighboring gene RNA, U6 small nuclear 602, pseudogene Neighboring gene ReSE screen-validated silencer GRCh37_chr14:32152531-32152718 Neighboring gene RNA, U6 small nuclear 455, pseudogene Neighboring gene NANOG hESC enhancer GRCh37_chr14:32179127-32179660 Neighboring gene MPRA-validated peak2132 silencer Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr14:32403751-32404407 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr14:32413341-32414540 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:32419941-32420560 Neighboring gene long intergenic non-protein coding RNA 2313 Neighboring gene ZFAND2A pseudogene 2

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_086410.1 

    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_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    31901685..31902884
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    26098999..26100198
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)