Deatailed information for cohesin site CDBP00417074


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  • Basic information
  • CohesinDB ID: CDBP00417074
  • Locus: chr21-32717971-32718233
  • Data sourse: GSE111537, GSE98367
  • Cell type: OCI-AML-3, Macrophage
  • 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): 0.978
  • Subunit: SA1,SA2,SMC1
  • 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: 90% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "5_TxWk": 59%, "15_Quies": 16%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: PGR, ZSCAN5C, ZNF660, SOX2, XBP1, HNF1A, PATZ1, FOXA1, ATF3, NFIC, ZFP64, ZNF362, ZBTB44, PRDM1, ATF4, MECOM, ZNF189, ZNF629, JMJD1C, TEAD1, KLF10, ESR1, MLL, CTCF, ZBTB20, TRIM24, ZNF528, TEAD4, KMT2B, TFAP2C, GLIS1, NANOG, CHD8, ZSCAN5D, ZNF778, ID3, ZSCAN21, ZBTB17, ZBTB48, ERG, ZBTB21, MYC, TSHZ1, RAD21, GRHL3, NKX2-1, GABPA, STAT3, NKX3-1, RCOR1, NR2F6, VDR, CEBPB, STAT5B, KMT2A, CREB1, EZH2, KLF8, FEZF1, GRHL2, ZHX2, SPI1, EHF, GATA2, FLI1, RUNX1, SMC1A, CEBPA, NKX2-2, AFF4, ZFX, SMAD3, ZBTB12, REPIN1, ZNF18, PRDM10, SMARCC1, ZNF35, ZNF384, OSR2, ZNF184, PBX4, ARNT, ATF2, ZEB2, SUPT5H, CDK8, ZXDB, MYB, SCRT2, PIAS1, SETDB1, NUP98-HOXA9, BCL11A, NR4A1, OVOL3, PHIP, PRDM6, ZNF394, SKI, FOXA2, TBL1X, EBF1, ZNF600, ZNF692, GTF2B, WT1, ZNF574, MEF2C, CDK9, ZNF580, HOXB13, RELA, HIF1A, TAL1, ZNF143, GATA1, TLE3, KLF4, SP7, ZNF213, MYOD1, ELF3, BRD2, AR, ZNF324, ZNF366, NOTCH3, SCRT1, BRD4, ZNF24
  • Target gene symbol (double-evidenced CRMs): URB1,SYNJ1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 20
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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