Deatailed information for cohesin site CDBP00420223


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  • Basic information
  • CohesinDB ID: CDBP00420223
  • Locus: chr21-42035231-42036340
  • Data sourse: GSE67783, GSE86191, GSE111913, GSE206145, GSE206145-NatGen2015
  • Cell type: RPE, Fibroblast, HCT-116, RT-112, 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): 0.944
  • Subunit: SA1,Rad21,SA2,SMC1
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: non-Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 94% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 63%, "14_ReprPCWk": 24%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, FOXA2, MYCN, SOX13, ZFX, XBP1, GTF2B, WT1, ZBTB48, MAFF, FOXA1, TET2, KDM1A, RARA, NEUROD1, SP140, ARNT, GABPA, NRIP1, NCOA3, TEAD3, ZMYM3, ESR1, CTCF, SOX5, RBM25, ZNF146, MAZ, NCOA2, STAG1, AHR
  • Target gene symbol (double-evidenced CRMs): PDE9A
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 2
  • Related genes and loops

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