Deatailed information for cohesin site CDBP00419180


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00419180
  • Locus: chr21-38448308-38449238
  • Data sourse: ENCSR000BLD, GSE101921, GSE138405, GSE115602
  • Cell type: MCF-7, H1-hESC, Hela-Kyoto, HCAEC
  • 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: Rad21,SA2,SMC1
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: non-Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 76% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 34%, "7_Enh": 19%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, SOX2, XBP1, PBX2, ATF3, CHD7, MORC2, JMJD1C, MAF, TRIM28, ETV1, LMO2, MLL, PITX3, JUN, TCF12, CTCF, EP300, SMC1, TEAD4, KMT2B, JARID2, NANOG, CHD8, ZSCAN5D, POU5F1, TOP2A, ZBTB17, ERG, PBX1, ASCL1, ETS1, RAD21, GABPA, STAT3, PRDM14, IKZF1, NFE2, CEBPB, KMT2A, CREB1, EZH2, SPI1, HDAC2, INTS13, FLI1, RUNX1, CEBPA, ZFX, ZNF534, SMAD3, HMGB2, ATF2, PBX3, MED1, TERF1, MYB, SMAD1, USF1, NIPBL, BCL11A, SP1, NR4A1, REST, ASH2L, BCOR, FOXP1, SMC3, NCOR2, STAG1, SKI, CBFA2T2, HOXB13, KDM1A, YY1, RELA, JUNB, MCM3, ZIC2, HIF1A, PCGF1, TAL1, MAX, KLF4, NCOA3, TP53, PKNOX1, MED, ZNF334, T, AR, HSF1, RNF2, BRD4, JUND
  • Target gene symbol (double-evidenced CRMs): ERG
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 88
  • Number of somatic mutations (non-coding): 8
  • Related genes and loops

eachgene