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LOC111589209 HNF4 motif-containing MPRA enhancer 232 [ Homo sapiens (human) ]

Gene ID: 111589209, updated on 10-Oct-2023

Summary

Gene symbol
LOC111589209
Gene description
HNF4 motif-containing MPRA enhancer 232
Gene type
biological region
Feature type(s)
regulatory: enhancer, transcriptional_cis_regulatory_region
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 predicted to be a cell type-specific enhancer based on chromatin state analysis from the ENCODE (ENCyclopedia Of DNA Elements) project. It was validated as a functional enhancer by high-throughput massively parallel reporter assays (MPRAs) in liver carcinoma HepG2 cells. This enhancer contains a motif for the HNF4 activator. Mutation of this motif results in reduced enhancer activity. [provided by RefSeq, Dec 2017]
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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 (153626998..153627142)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) X NC_060947.1 (151900634..151900778)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) X NC_000023.10 (152892453..152892597)

Chromosome X - NC_000023.11Genomic Context describing neighboring genes Neighboring gene keratin 18 pseudogene 48 Neighboring gene MRFAP1 pseudogene 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 21067 Neighboring gene H3K4me1 hESC enhancer GRCh37_chrX:152888899-152889398 Neighboring gene dual specificity phosphatase 9 Neighboring gene ribosomal protein L18a pseudogene 16

Genomic regions, transcripts, and products

General gene information

Other Names

  • HNF4 activator MPRA enhancer 232
  • massively parallel reporter assay enhancer 232

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_056080.1 

    Range
    101..245
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    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
    153626998..153627142
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060947.1 Alternate T2T-CHM13v2.0

    Range
    151900634..151900778
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    GenBank, FASTA, Sequence Viewer (Graphics)