Deatailed information for cohesin site CDBP00415192


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00415192
  • Locus: chr21-25254396-25255340
  • Data sourse: GSE115248, GSE126634, ENCSR404BPV, GSE152721, ENCSR198ZYJ, ENCSR000EHX
  • Cell type: Kelly, Neurons-H1, HAP1, SK-N-SH
  • 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): 0.956
  • Subunit: SMC3,Rad21,SMC1
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: False Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 35% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 89%, "9_Het": 8%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXA2, MYCN, TOP2A, NME2, FOXA1, TWIST1, HNF4G, KDM1A, NEUROD1, EOMES, SMARCA4, ISL1, GRHL3, OTX2, GATA3, RCOR1, HAND2, ESR1, PITX3, SETDB1, EBF3, PHOX2B, T, EP300, AR, GATA6, GATA2, REST, TEAD4, TBX2
  • 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

eachgene