Deatailed information for cohesin site CDBP00416796


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  • Basic information
  • CohesinDB ID: CDBP00416796
  • Locus: chr21-31983009-31983792
  • Data sourse: ENCSR000BLD, ENCSR167MTG, ENCSR000EEG, ENCSR230ZWH, GSE67783, GSE72082, GSE138405, GSE86191, ENCSR000BLY, ENCSR000BLS, GSE105028, ENCSR054FKH, ENCSR000EHX, ENCSR635OSG, ENCSR703TNG, GSE25021, GSE116344, ENCSR000EDW, ENCSR917QNE
  • Cell type: MCF-7, H1-hESC, Hela-Kyoto, HCT-116, RH4, Hep-G2, SK-N-SH, Liver, HSPC, H9-hESC
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 7% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.889
  • Subunit: SMC3,Rad21,SA2,SA1
  • CTCF binding site: CTCF CTCF motif: True
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 71% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 57%, "5_TxWk": 22%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: NCOA2, EZH2phosphoT487, PGR, SMC1A, POU2F2, HMG20A, CHD8, CEBPA, FOXA2, SOX13, ZFX, ZNF649, XBP1, HNF1A, ZBTB48, WT1, FOXA1, ZBTB33, DDX5, SAP130, HOXB13, ZKSCAN1, ZNF496, ERG, YY1, RELA, CREBBP, ZBTB2, ATF3, AHR, CTCFL, RAD21, GRHL3, RXRA, GATA3, ZNF48, SMAD4, MAX, NRIP1, DACH1, NR2F6, MED1, ZNF736, NR3C1, CEBPB, CEBPG, TEAD3, NR2F2, NCOA3, CEBPD, NR2F1, EZH2, ESR1, PHOX2B, CTCF, ELF3, USF1, SP1, SPI1, RBM22, HNF4A, LMO1, AR, ARID4B, SOX5, BCL11A, REST, JUND, SMC3, STAG1, TFAP2C
  • Target gene symbol (double-evidenced CRMs): SYNJ1,HUNK,CFAP298-TCP10L,MIS18A,CFAP298
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 15
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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