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LOC124629409 Sharpr-MPRA regulatory region 12950 [ Homo sapiens (human) ]

Gene ID: 124629409, updated on 10-Oct-2023

Summary

Gene symbol
LOC124629409
Gene description
Sharpr-MPRA regulatory region 12950
Gene type
biological region
Feature type(s)
regulatory: silencer
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 repressive element 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 Repressive DNase matched - State 8:EnhW, candidate weak enhancer and open chromatin). [provided by RefSeq, Mar 2022]
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Genomic context

Location:
12q
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 12 NC_000012.12 (75888009..75888303)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 12 NC_060936.1 (75863090..75863384)

Chromosome 12 - NC_000012.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105369844 Neighboring gene uncharacterized LOC124900321 Neighboring gene NANOG hESC enhancer GRCh37_chr12:76105024-76105525 Neighboring gene NANOG hESC enhancer GRCh37_chr12:76140468-76140969 Neighboring gene uncharacterized LOC105369846 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 4663 Neighboring gene Sharpr-MPRA regulatory region 6163 Neighboring gene Sharpr-MPRA regulatory region 14186 Neighboring gene Sharpr-MPRA regulatory region 2424 Neighboring gene H3K27ac hESC enhancer GRCh37_chr12:76351262-76352207 Neighboring gene NOP10 ribonucleoprotein homolog (yeast) pseudogene Neighboring gene RNA, 7SL, cytoplasmic 734, pseudogene

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_079768.1 

    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_000012.12 Reference GRCh38.p14 Primary Assembly

    Range
    75888009..75888303
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060936.1 Alternate T2T-CHM13v2.0

    Range
    75863090..75863384
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)