Deatailed information for cohesin site CDBP00417776


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00417776
  • Locus: chr21-34593440-34593796
  • Data sourse: ENCSR153HNT, GSE86191
  • Cell type: K-562, HCT-116
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 0% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.978
  • Subunit: SA1,Rad21
  • CTCF binding site: non-CTCF CTCF motif: False
  • 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: 93% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 42%, "7_Enh": 32%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: XBP1, FOXA1, PBX2, UBTF, ZFHX2, THAP1, CDX2, KLF5, TRIM28, ETV1, NFE2L2, CTCF, JUN, EP300, KLF1, BAF155, DPF2, TEAD4, GATAD2A, PDX1, ZSCAN5D, POU5F1, MYCN, ID3, CTBP1, ZNF317, ZBTB48, DUX4, STAT1, SAP130, ERG2, ASCL1, MYC, RAD21, FOXP2, GRHL3, RXRA, XRCC5, ZNF614, RCOR1, NFE2, HNRNPH1, NR3C1, CEBPB, HNRNPL, ZBTB11, TBL1XR1, PHF8, GATA2, ATF1, RUNX1, CTNNB1, BCL6, ZNF585A, HDAC1, LDB1, NKX2-2, CBX1, SOX13, ZFX, TET2, ERG3, SMARCC1, MEF2A, RARA, ZNF384, RUNX2, GATA4, ARNT, PRDM9, CBFA2T3, MED1, ZMYM3, SMAD1, KLF9, TBX5, RBM22, BCL11A, SP1, HNF4A, NKX2-5, ZBTB7A, RBM25, ATF7, HNRNPLL, BCOR, SMC3, STAG1, TRP47, KLF13, PPARG, CBX3, MTA3, CREM, FOXA2, SS18, WT1, FOXF1, ZNF823, KDM1A, YY1, RELA, NEUROD1, SP140, ZFP36, OTX2, TAL1, MAX, GATA1, GFI1B, NR2F2, PKNOX1, ZNF334, EGR2, BRD2, BHLHE40, AR, RXR, EGR1, ZBTB26, RNF2, MYNN, BRD4, ILF3, JUND, CLOCK, MAZ, MEF2D
  • Target gene symbol (double-evidenced CRMs): SMIM11A,RCAN1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 3
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

eachgene