Deatailed information for cohesin site CDBP00417127


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  • Basic information
  • CohesinDB ID: CDBP00417127
  • Locus: chr21-32911935-32912474
  • Data sourse: GSE67783, GSE86191, GSE138405, GSE110061, GSE129526, GSE105028, ENCSR153HNT, ENCSR000EDE, GSE25021, GSE50893
  • Cell type: MCF-7, Hela-Kyoto, HCT-116, HeLa-S3, K-562, HSPC, GM18486, H9-hESC
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 2% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.911
  • Subunit: SA1,Rad21,SA2
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: TES
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 89% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 61%, "14_ReprPCWk": 36%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: MEIS2, ZFX, FOXA1, SRF, PBX2, ARID3A, ATF3, CTCFL, RAD21, ARID1B, CBFA2T3, GATA1, DACH1, ESRRA, ZNF512, EZH2, ESR1, CTCF, BCL11A, TEAD4, STAG1
  • Target gene symbol (double-evidenced CRMs): IFNGR2,TMEM50B
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 7
  • Related genes and loops

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