Deatailed information for cohesin site CDBP00418767


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00418767
  • Locus: chr21-37197105-37197434
  • Data sourse: GSE67783, GSE86191
  • Cell type: HCT-116, HSPC
  • 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: TSS
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 90% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "4_Tx": 64%, "5_TxWk": 31%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, FOSL1, PGR, XBP1, FOXA1, LEO1, MLL4, ZFHX2, ATF3, ZFP64, PRDM1, ZNF532, ZNF736, CDX2, KLF5, ELF1, TEAD1, KLF6, ESR1, OCA2, HNF1B, CTCF, TCF12, JUN, EP300, NUTM1, SOX9, SOX4, E2F1, TEAD4, TFAP2C, GLIS1, POU2F2, CHD8, ZSCAN5D, MYCN, ZNF263, POU5F1, RUNX1T1, CDK7, ZBTB48, ZSCAN5A, ERG2, HOXC5, ERG, OGG1, MYC, SMARCA4, EOMES, RAD21, LHX2, GRHL3, TOP1, PROX1, RXRA, APC, STAT3, SOX10, RCOR1, NR3C1, CEBPB, SRSF3, EZH2, SPI1, IRF1, MXD3, NCOA2, ETV5, RUNX1, CTNNB1, BCL6, CEBPA, ZFX, SMAD3, TET2, ERG3, NSD2, ZNF384, TAF15, RUNX2, CDK6, GATA4, OSR2, GR, ARNT, DAXX, PBX4, NRF1, PRDM9, FOXM1, FOS, SUPT5H, TEAD3, ZEB1, ZNF3, KLF9, ZNF41, RBM22, BCL11A, NIPBL, SP1, HNF4A, GSPT2, ZBTB7A, HNRNPLL, PHIP, FOXP1, AATF, SMC3, STAG1, TRP47, PPARG, FOXA2, CBX3, AGO1, TBL1X, PAF1, WT1, YY1, RELA, NEUROD1, JUNB, SP140, TCF4, HIF1A, OTX2, TAL1, MAX, ZNF143, AGO2, CBX2, KLF4, SP7, NCOA3, NEUROG2, NR2F1, TP53, MYOD1, ELF3, BRD2, BHLHE40, PAX3-FOXO1, AR, ZBTB16, RXR, EGR1, ZBTB26, NCOR1, HSF1, BRD4, JUND, MAZ, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): KCNJ6,TTC3
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 3
  • Number of somatic mutations (non-coding): 1
  • Related genes and loops

eachgene