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LOC132088611 Neanderthal introgressed variant-containing enhancer experimental_1658 [ Homo sapiens (human) ]

Gene ID: 132088611, updated on 12-Sep-2024

Summary

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Gene symbol
LOC132088611
Gene description
Neanderthal introgressed variant-containing enhancer experimental_1658
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 both the introgressed and non-introgressed 1:20408831 variant alleles. [provided by RefSeq, Sep 2023]
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Genomic context

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See LOC132088611 in Genome Data Viewer
Location:
chromosome: 1
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (20082253..20082422)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (19905889..19906058)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (20408746..20408915)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:20304755-20305254 Neighboring gene phospholipase A2 group IIA Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1574 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:20316184-20316758 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:20316759-20317334 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1580 Neighboring gene prenylcysteine oxidase 1 pseudogene Neighboring gene phospholipase A2 group V Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1609 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1624 Neighboring gene Sharpr-MPRA regulatory region 6877 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1646 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1651 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 310 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 311 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 312 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1659 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1661 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1663 Neighboring gene Neanderthal introgressed variant-containing enhancer experimental_1667 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 313 Neighboring gene phospholipase A2 group IID Neighboring gene ATAC-STARR-seq lymphoblastoid active region 314 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 315 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:20468424-20468924 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:20474795-20475295 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:20476004-20476630 Neighboring gene phospholipase A2 group IIF

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Detection of Neanderthal Adaptively Introgressed Genetic Variants That Modulate Reporter Gene Expression in Human Immune Cells. Jagoda E, et al. Mol Biol Evol, 2022 Jan 7. PMID 34662402, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See Variation Viewer (GRCh37.p13)

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_229170.1 

    Range
    101..270
    Download
    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_000001.11 Reference GRCh38.p14 Primary Assembly

    Range
    20082253..20082422
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060925.1 Alternate T2T-CHM13v2.0

    Range
    19905889..19906058
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    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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