Deatailed information for cohesin site CDBP00417458


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00417458
  • Locus: chr21-33735737-33735979
  • Data sourse: GSE67783, GSE86191
  • Cell type: HCT-116, HSPC
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 0% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.978
  • Subunit: SA1,Rad21
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: non-Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 88% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "5_TxWk": 52%, "15_Quies": 30%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, FOXA2, POU5F1, MEIS1, TOP2A, ZSCAN16, STAT1, FOXA1, CBX8, ERG3, MEF2C, CDK9, SP4, CREBBP, ZNF384, MYC, RUNX2, GATA4, SMARCA4, ZFP64, SP140, PRDM9, TAL1, ETV6, MED1, NR3C1, CEBPB, TRIM28, EBF3, ZNF22, CTCF, SPI1, AR, PAX8, IRF4, RNF2, SCRT1, BRD4, ZNF766, E2F1
  • Target gene symbol (double-evidenced CRMs): AP000311.1,CRYZL1,ITSN1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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