Deatailed information for cohesin site CDBP00419460


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  • Basic information
  • CohesinDB ID: CDBP00419460
  • Locus: chr21-39332176-39332684
  • Data sourse: ENCSR000BLD, GSE206145-GSE177045, ENCSR000FAD, GSE105028, ENCSR153HNT
  • Cell type: K-562, H1-hESC, MCF-7, H9-hESC
  • 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): 0.956
  • Subunit: Mau2,SA1,Rad21
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intergenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 91% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 59%, "5_TxWk": 18%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, SOX2, XBP1, FOXA1, PBX2, RXRB, TFAP4, HDGF, CHD7, PRDM1, ZNF189, SMARCE1, PAX5, ZNF320, CDX2, TEAD1, NFE2L2, ESR1, OCA2, CTCF, TCF12, JUN, EP300, E4F1, GATA6, DPF2, SOX6, E2F1, GATAD2A, GLIS1, NANOG, ID3, CTBP1, MTA2, ZBTB48, SAP130, MYC, SMARCA4, EOMES, ARID1B, RAD21, GRHL3, FOXK2, STAT3, XRCC5, IKZF1, RCOR1, NR2F6, CEBPB, ESRRA, CREB1, ELF4, SPI1, HDAC2, GATA2, SMARCA5, NFIL3, ZNF554, ATF1, ETV5, BCL6, CEBPA, HDAC1, ZFX, SMAD3, ZNF770, RARA, CREBBP, SMAD2, GATA4, OSR2, ZEB2, SMAD4, ETV6, NR2C1, ZNF10, MED1, TEAD3, L3MBTL2, BCL11A, GSPT2, HNF4A, REST, ZBTB7A, MLLT1, MTA3, RBBP5, ZNF30, WT1, ZBTB33, ZNF580, KDM1A, YY1, RELA, JUNB, ZIC2, HIF1A, GATA3, MAX, NRIP1, GATA1, MTA1, ZNF143, HAND2, GFI1B, NCOA3, NR2F1, PKNOX1, MYOD1, T, BRD2, ELF3, PTRF, ZBTB40, ZBTB42, RNF2, BRD4, JUND, ILF3, MAZ
  • Target gene symbol (double-evidenced CRMs): SH3BGR,LCA5L,GET1,GET1-SH3BGR,ETS2
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 3
  • Related genes and loops

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