Deatailed information for cohesin site CDBP00416698


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  • Basic information
  • CohesinDB ID: CDBP00416698
  • Locus: chr21-31706429-31706648
  • Data sourse: GSE206145-NatGen2015, GSE86191
  • Cell type: Fibroblast, HCT-116
  • 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: Rad21,SA2
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: TSS,TES
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 67% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "5_TxWk": 71%, "7_Enh": 17%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: CHD8, FOXA2, PAF1, POU4F2, ZBTB48, WT1, FOXA1, FOXF1, LEO1, ERG, YY1, RELA, HDGF, MYC, SP140, GRHL3, PRDM1, PRDM9, TAL1, SUPT5H, AGO2, GATA1, MED1, NR2F1, EZH2, KDM5B, OCA2, FEZF1, RBM22, ZNF324, HSF1, NOTCH3, BRD4, MAZ, RELB, TEAD4, AHR
  • Target gene symbol (double-evidenced CRMs): TIAM1,SCAF4,SYNJ1,CFAP298,CFAP298-TCP10L
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 3
  • Number of somatic mutations (non-coding): 1
  • Related genes and loops

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