Deatailed information for cohesin site CDBP00417220


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  • Basic information
  • CohesinDB ID: CDBP00417220
  • Locus: chr21-33157388-33157662
  • Data sourse: ENCSR000BLD, GSE105028, ENCSR153HNT, GSE138405
  • Cell type: K-562, H1-hESC, Hela-Kyoto, H9-hESC
  • 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): 0.956
  • Subunit: SA1,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: 93% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "14_ReprPCWk": 62%, "15_Quies": 22%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: NANOG, FOXA2, ZNF263, CDK7, SIN3A, MIER2, GTF2B, ZBTB17, PCBP2, STAT1, FOXA1, ERG3, ERG2, SP4, CDK9, ZFHX2, TBP, ZNF596, YY1, HOXB13, MIER1, MYC, PRDM1, SP3, HIF1A, GABPA, MAX, ZNF398, FOS, GATA1, MED1, ARNTL, ZNF467, TRIM28, SCRT2, EZH2, MLLT1, KDM5B, KLF8, SAP30, ZBTB6, ESR1, ZSCAN22, EGR2, PHOX2B, SP1, KLF1, BAF155, BCL11A, HDAC2, REST, EGLN2, ZNF366, SIX2, HSF1, BRD4, AFF1, BCOR, FOXP1, MAZ, TEAD4, ZNF24, EHMT2
  • Target gene symbol (double-evidenced CRMs): SYNJ1
  • 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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