Deatailed information for cohesin site CDBP00414496


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  • Basic information
  • CohesinDB ID: CDBP00414496
  • Locus: chr21-21061987-21065549
  • Data sourse: GSE206145-GSE177045, GSE72082, GSE76893, ENCSR703TNG, GSE25021
  • Cell type: MCF-7
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 4% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.989
  • Subunit: NIPBL,SA1,Rad21,SMC1,Mau2
  • 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: False ChIA-PET loops: True
  • Compartment: 27% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 85%, "5_TxWk": 6%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: PGR, SMC1A, CBX1, TOP2A, SIN3A, CTBP1, SMAD3, FOXA1, HOXB13, ERG, CREBBP, MEN1, AHR, MYC, RUNX2, GR, RAD21, ARNT, HIF1A, GATA3, GABPA, STAT3, SMARCE1, NRIP1, ZNF143, NKX3-1, CDK8, HDAC3, MED1, TLE3, NR3C1, ESRRA, NCOA3, TEAD1, ELF1, ETV1, PIAS1, NR2F1, KDM5B, ZNF217, ESR1, TCF7L2, TP73, LMO2, GRHL2, TRPS1, TCF12, EP300, BAF155, NIPBL, HNF4A, AR, TFAP2A, DPF2, ZBTB40, GATA2, ZNF479, ZBTB7A, EGLN2, FLI1, ASH2L, JUND, BRD4, CTBP2, FOXP1, CUX1, MBD2, NCOA2, STAG1, TFAP2C
  • Target gene symbol (double-evidenced CRMs): NCAM2
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 49
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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