Deatailed information for cohesin site CDBP00417152


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00417152
  • Locus: chr21-32986202-32986308
  • Data sourse: GSE120943, GSE98367
  • Cell type: Monocytes, Macrophage
  • 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: SMC1
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 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: "14_ReprPCWk": 65%, "15_Quies": 26%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: POU2F2, CHD8, MYCN, ZNF263, KDM4C, ZFX, NME2, XBP1, DUX4, FOXA1, FOXF1, YY1, RELA, ZNF384, PBX1, ATF3, EOMES, GRHL3, ATF2, ZSCAN4, GATA1, ZNF143, ZFP69B, CREB1, SCRT2, NEUROG2, EZH2, ZNF334, JUN, CTCF, SPI1, AR, PAX3-FOXO1, TAF1, NOTCH3, BRD4, SCRT1, TCF3, CLOCK, SMC3
  • Target gene symbol (double-evidenced CRMs): TMEM50B,IFNGR2
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

eachgene