Deatailed information for cohesin site CDBP00419918


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00419918
  • Locus: chr21-41159227-41159964
  • Data sourse: GSE67783, GSE86191
  • Cell type: HCT-116, HSPC
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 1% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.978
  • Subunit: SA1,Rad21
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intergenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 67% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 41%, "14_ReprPCWk": 36%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: NCOA2, CBX3, CEBPA, MYCN, POU5F1, RUNX1T1, ZFX, XBP1, WT1, SUZ12, RELA, JUNB, MYC, PBX4, GRHL3, CBFB, TAL1, FOS, ZNF736, CEBPG, CEBPB, NCOA3, CEBPD, TRIM28, CREB1, TFAP2C, EZH2, ESR1, ZNF334, NFKB1, SETDB1, JUN, CTCF, AR, ATF7, NOTCH3, BRD4, ZNF528, MAZ, SMC3, STAG1, AHR
  • Target gene symbol (double-evidenced CRMs): FAM3B,TMPRSS2,PRDM15,MX2,MX1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 4
  • Related genes and loops

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