Deatailed information for cohesin site CDBP00414169


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  • Basic information
  • CohesinDB ID: CDBP00414169
  • Locus: chr21-18603256-18603658
  • Data sourse: GSE152721, ENCSR198ZYJ, ENCSR404BPV
  • Cell type: Neurons-H1, HAP1
  • 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: SMC3,Rad21
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 30% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 80%, "7_Enh": 9%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: POU2F2, MAFG, CEBPA, FOXA2, NKX2-2, NME2, MAFF, FOXA1, CDK9, HOXB13, ERG, RELA, ZNF90, NFKB2, MYC, SMARCA4, CHD7, ARNT, GRHL3, ATF2, GABPA, MAX, CDK8, MED1, TFAP2C, EZH2, C11orf30, GRHL2, NFKB1, PHOX2B, BRD2, NUP98-HOXA9, MAFK, AR, REST, IRF4, HSF1, BRD4, JUND, ZNF316
  • Target gene symbol (double-evidenced CRMs): .
  • 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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