Deatailed information for cohesin site CDBP00415519


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00415519
  • Locus: chr21-26570205-26570607
  • Data sourse: GSE101921, GSE94872, ENCSR230ZWH, ENCSR917QNE
  • Cell type: Liver, HUVEC, HCAEC
  • 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): 0.967
  • Subunit: Rad21,SMC1
  • 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: True ChIA-PET loops: True
  • Compartment: 42% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 41%, "14_ReprPCWk": 21%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: TRIM25, SOX2, XBP1, FOXA1, SUZ12, TFAP4, ZNF90, ATF3, CTCFL, CHD7, CBFB, TP63, ZNF736, TRIM28, ETV1, ESR1, OCA2, MED26, JUN, CTCF, TCF12, EP300, RYBP, E2F6, E2F1, SMC1, TEAD4, GTF2F1, PDX1, TFAP2C, EED, JARID2, NANOG, CHD8, BRD1, ZSCAN5D, POU5F1, MYCN, BRD3, KDM4C, ZBTB48, STAT1, SRF, TBP, ERG, OGG1, ETS1, MYC, SMARCA4, KDM4A, RAD21, GRHL3, RXRA, STAT3, PRDM14, NFE2, NR3C1, SRSF3, KMT2A, CREB1, EZH2, PHF8, ZHX2, SPI1, HDAC2, GATA2, INTS13, SIX2, FLI1, MXI1, HCFC1R1, MRTFB, PTBP1, RUNX1, SMC1A, EZH2phosphoT487, NKX2-2, SIRT6, SIN3A, ZFX, SMAD3, TET2, RARA, ZNF384, RUNX2, BACH1, ETV6, MAFB, CHD1, CDK8, CEBPD, TAF7, SETDB1, USF1, SP1, BCL11A, REST, ARID1A, ASH2L, PCGF2, CTBP2, BCOR, FOXP1, AATF, SMC3, STAG1, STAG2, TRP47, FOXA2, TBL1X, RBBP5, EBF1, NFATC1, ZNF207, WT1, HOXB13, KDM1A, YY1, RELA, ZNF19, NEUROD1, SP140, HIF1A, PCGF1, OTX2, TAL1, MAX, MAF1, GATA1, ZNF143, AGO2, CBX2, NR2F2, KDM5B, TP53, BRD2, T, AR, TAF1, RXR, HEXIM1, HSF1, NOTCH3, BRD4, JUND, MAZ, ZNF316
  • Target gene symbol (double-evidenced CRMs): CYYR1,APP
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 22
  • Number of somatic mutations (non-coding): 11
  • Related genes and loops

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