Deatailed information for cohesin site CDBP00419622


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  • Basic information
  • CohesinDB ID: CDBP00419622
  • Locus: chr21-39881640-39882899
  • Data sourse: ENCSR000BLD, ENCSR000BTQ, GSE72082, GSE25021, GSE105028, ENCSR000ECE, GSE50893, GSE83726, ENCSR703TNG, GSE145327, GSE116344, GSE97394
  • Cell type: MCF-7, H1-hESC, RH4, GM2588, H9-hESC, HUES64
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 4% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.933
  • Subunit: SA1,Rad21
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: False Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 48% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 63%, "14_ReprPCWk": 17%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: POU2F2, EZH2phosphoT487, NKX2-2, MYCN, TOP2A, ZFX, SMAD3, FOXA1, SUZ12, CDK9, ERG, RELA, NFKB2, AHR, RUNX2, MYC, RAD21, GRHL3, HIF1A, ARNT, OTX2, MAFB, MITF, MED1, MYOG, NCOA3, CREB1, EZH2, TP53, OCA2, KLF9, GRHL2, NFKB1, MYOD1, CTCF, JUN, IRF4, BRD4, RELB, SMC3, STAG1, RBPJ
  • Target gene symbol (double-evidenced CRMs): PCP4
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 14
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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