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LOC113875036 Sharpr-MPRA regulatory region 14511 [ Homo sapiens (human) ]

Gene ID: 113875036, updated on 10-Oct-2023

Summary

Gene symbol
LOC113875036
Gene description
Sharpr-MPRA regulatory region 14511
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 sequence was predicted to be a transcriptional regulatory region based on chromatin state analysis from the ENCODE (ENCyclopedia Of DNA Elements) project. It was validated as a functional enhancer by the Sharpr-MPRA technique (Systematic high-resolution activation and repression profiling with reporter tiling using massively parallel reporter assays) in K562 erythroleukemia cells (group: K562 Activating DNase unmatched - State 24:Quies, heterochromatin/dead zone), with weaker activation in HepG2 liver carcinoma cells (group: HepG2 Activating non-DNase unmatched - State 24:Quies). [provided by RefSeq, Dec 2018]
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Genomic context

Location:
Xq
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) X NC_000023.11 (67780807..67781101)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (66212797..66213091)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (67000649..67000943)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene poly(A) binding protein nuclear 1 pseudogene Neighboring gene androgen receptor repeat instability region Neighboring gene androgen receptor Neighboring gene negative expression of androgen receptor regulating lncRNA Neighboring gene BMI1 proto-oncogene, polycomb ring finger pseudogene 1 Neighboring gene NANOG hESC enhancer GRCh37_chrX:67280228-67280729 Neighboring gene oligophrenin 1 Neighboring gene phosphoglycerate kinase 1 pseudogene 1

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_063224.1 

    Range
    101..395
    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_000023.11 Reference GRCh38.p14 Primary Assembly

    Range
    67780807..67781101
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    66212797..66213091
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    GenBank, FASTA, Sequence Viewer (Graphics)