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LOC127401858 H3K4me1 hESC enhancer GRCh37_chr4:165304399-165304900 [ Homo sapiens (human) ]

Gene ID: 127401858, updated on 12-Sep-2024

Summary

Gene symbol
LOC127401858
Gene description
H3K4me1 hESC enhancer GRCh37_chr4:165304399-165304900
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 ChIP-STARR-seq massively parallel reporter assay in primed human embryonic stem cells. This enhancer is marked by the H3K4me1 histone modification. [provided by RefSeq, Oct 2022]
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Genomic context

See LOC127401858 in Genome Data Viewer
Location:
chromosome: 4
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (164383247..164383748)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (167730916..167731417)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (165304399..165304900)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene membrane associated ring-CH-type finger 1 Neighboring gene heat shock protein family A (Hsp70) member 5 pseudogene Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165162454-165162964 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165162965-165163475 Neighboring gene acidic nuclear phosphoprotein 32 family member C, pseudogene Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr4:165272175-165272792 Neighboring gene MPRA-validated peak5144 silencer Neighboring gene RNA, U6 small nuclear 284, pseudogene Neighboring gene H3K4me1 hESC enhancer GRCh37_chr4:165597429-165597929 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_75752 Neighboring gene CHORDC1 pseudogene 3

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_103818.1 

    Range
    101..602
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    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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
    164383247..164383748
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    167730916..167731417
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)