Deatailed information for cohesin site CDBP00413337


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00413337
  • Locus: chr21-14824996-14827058
  • Data sourse: ENCSR000EAC, ENCSR000DZP, GSE155324, ShirahigeLab, ShirahigeLab-NatGen2015, ENCSR000BMY, GSE50893
  • Cell type: GM2630, Fibroblast, SNYDER, GM10847, Lymphoblast, GM19240, GM12878, GM12891, GM2255, GM19239, GM19193, B-cell
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 4% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.867
  • Subunit: Mau2,SMC3,Rad21,SA1
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: TSS,TES
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 47% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 95%, "7_Enh": 3%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: NFATC3, RUNX1, POU2F2, MEF2B, SMC1A, HDAC1, MTA3, CREM, EBF1, NFATC1, RUNX1T1, MTA2, GTF2B, FOXA1, ZNF205, TCF7, NBN, ARID3A, TRIM22, BCL3, PRDM10, HNRNPK, MEF2A, RELA, HDGF, TARDBP, YY1, ZNF597, JUNB, TSC22D4, NFIC, MYC, ARID1B, RUNX3, PRDM1, SKIL, ATF2, BATF3, BATF, TAL1, FOXM1, CBFA2T3, MAX, GATA1, IKZF1, MED1, BACH2, PML, BCLAF1, TRIM28, CREB1, ZMYM3, SMAD1, ZNF687, NFKB1, STAT5A, ZFP91, CTCF, TCF12, RBM22, BCL11A, SPI1, TBX21, SP1, SND1, IRF1, DPF2, HDAC2, IRF4, ATF7, ASH2L, RAD51, IKZF2, BRD4, HSF1, RELB, MLLT1, RBPJ, EED
  • Target gene symbol (double-evidenced CRMs): SAMSN1,HSPA13
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 4
  • Related genes and loops

eachgene