Deatailed information for cohesin site CDBP00421348


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  • Basic information
  • CohesinDB ID: CDBP00421348
  • Locus: chr21-45789051-45790732
  • Data sourse: GSE67783, GSE86191, GSE206145, GSE206145-NatGen2015, ENCSR153HNT
  • Cell type: RPE, Fibroblast, HCT-116, K-562, HSPC
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 2% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.944
  • Subunit: SA1,Rad21,SA2
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 83% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 45%, "14_ReprPCWk": 26%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, XBP1, FOXA1, SUZ12, ATF3, MORC2, TP63, ZSCAN4, ZNF467, ESR1, OCA2, TP73, CTCF, JUN, EP300, MNT, PAX8, RFX5, TFAP2C, EED, POU2F2, CHD8, MYCN, ZNF263, ZBTB48, STAT1, ERG, USP7, MYC, GRHL3, RXRA, STAT3, DNMT3B, ARNTL, NR3C1, CREB1, EZH2, SPI1, IRF1, SSRP1, NCOA2, ETV5, PTBP1, RUNX1, SMC1A, BCL6, EZH2phosphoT487, CRY1, ZFX, POU4F2, TET2, ERG3, ARNT, ETV6, PBX3, FOS, CDK8, BCL11A, REST, TCF3, AATF, SMC3, STAG1, TRP47, NFATC1, WT1, BCL3, KDM1A, YY1, RELA, JUNB, SP140, HIF1A, MAX, NRIP1, ZNF143, GATA1, CBX2, NCOA3, NR2F1, TP53, MYOD1, AR, HSF1, NCOR1, BRD4, JUND, CLOCK, MAZ, AHR
  • Target gene symbol (double-evidenced CRMs): SLC19A1,PCBP3
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 23
  • Number of somatic mutations (non-coding): 23
  • Related genes and loops

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