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LOC132089409 Neanderthal introgressed variant-containing enhancer experimental_92203 [ Homo sapiens (human) ]

Gene ID: 132089409, updated on 12-Sep-2024

Summary

Gene symbol
LOC132089409
Gene description
Neanderthal introgressed variant-containing enhancer experimental_92203
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 contains a Neanderthal adaptively introgressed genetic variant, and was validated as an enhancer by massively parallel reporter assays (MPRAs) in K562 erythroleukemia cells, with activity observed for the non-introgressed 6:53147972 variant allele. [provided by RefSeq, Sep 2023]
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Genomic context

See LOC132089409 in Genome Data Viewer
Location:
chromosome: 6
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 6 NC_000006.12 (53283089..53283258)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 6 NC_060930.1 (53122847..53123016)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 6 NC_000006.11 (53147887..53148056)

Chromosome 6 - NC_000006.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124901332 Neighboring gene ELOVL fatty acid elongase 5 Neighboring gene microRNA 5685 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24694 Neighboring gene NANOG-H3K27ac hESC enhancer GRCh37_chr6:53169169-53169692 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24695 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24696 Neighboring gene Sharpr-MPRA regulatory region 4240 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 24697 Neighboring gene ribosomal protein S16 pseudogene 5 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 17289 Neighboring gene ribosomal protein L31 pseudogene 28

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_229968.1 

    Range
    101..270
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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_000006.12 Reference GRCh38.p14 Primary Assembly

    Range
    53283089..53283258
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060930.1 Alternate T2T-CHM13v2.0

    Range
    53122847..53123016
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)