Deatailed information for cohesin site CDBP00421032


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  • Basic information
  • CohesinDB ID: CDBP00421032
  • Locus: chr21-44534275-44535130
  • Data sourse: GSE110061, GSE67783, GSE126755, ENCSR153HNT
  • Cell type: K-562, HCT-116, HSPC, Neutrophil
  • 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): 0.956
  • Subunit: SA1,Rad21,SMC3
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: TSS,TES
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 80% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 50%, "14_ReprPCWk": 32%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: RUNX1, PGR, MAFG, MYCN, POU5F1, WT1, MAFF, MEF2C, HOXB13, KDM1A, ETS1, MYC, AHR, CTCFL, ARNT, ZNF189, MTA1, NFE2, RCOR1, TEAD1, ZNF121, CREB1, ZMYM3, ZNF3, KLF8, C11orf30, CTCF, MAFK, SPI1, KLF1, ZNF146, ILF3, TEAD4, GTF2F1, ZNF316
  • Target gene symbol (double-evidenced CRMs): COL18A1,TSPEAR
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 9
  • Number of somatic mutations (non-coding): 3
  • Related genes and loops

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