Deatailed information for cohesin site CDBP00421076


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  • Basic information
  • CohesinDB ID: CDBP00421076
  • Locus: chr21-44686092-44689539
  • Data sourse: ENCSR000BLD, ENCSR167MTG, GSE131606, GSE206145-GSE177045, GSE67783, GSE72082, GSE86191, GSE25021, ENCSR000BLS, GSE105028, GSE206145-NatGen2015, ENCSR000ECE, ENCSR054FKH, GSE206145, GSE83726, GSE106870, GSE50893, GSE145327, GSE97394
  • Cell type: MCF-7, H1-hESC, RPE, Fibroblast, HCT-116, RH4, Hep-G2, GM2610, CVB-hiPSC, HUES64, H9-hESC, CVI-hiPSC, HSPC, DKO
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 6% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.844
  • Subunit: Mau2,SA1,Rad21,SA2
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: TSS,TES
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 80% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "14_ReprPCWk": 41%, "13_ReprPC": 23%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, TRIM25, SOX2, XBP1, FOXA1, SUZ12, ATF3, RUNX3, CHD7, CBFB, MECOM, PAX5, TP63, TEAD1, BCLAF1, TRIM28, RBM39, ELF1, ESR1, OCA2, USF2, CTCF, TCF12, EP300, POU2F1, GATA6, DPF2, SOX4, E2F6, E2F4, TEAD4, PDX1, TFAP2C, EED, GLIS1, JARID2, NANOG, CHD8, ZNF425, BRD1, MYCN, POU5F1, RUNX1T1, ZNF263, ZBTB48, ZSCAN5A, ERG, ASCL1, OGG1, MYC, EZH1, SMARCA4, EOMES, FOXP2, RAD21, GRHL3, NKX2-1, GABPA, STAT3, PRDM14, IKZF1, VDR, NR3C1, STAT5B, CREB1, EZH2, GRHL2, SPI1, HDAC2, GATA2, GATAD2B, SIX2, FLI1, RELB, NCOA2, MYF5, RUNX1, SIRT6, EZH2phosphoT487, SIN3A, ZFX, ZNF335, POU4F2, SMAD3, TET2, SMARCC1, RARA, TAF15, SMAD2, ARNT, BACH1, PRDM9, SMAD4, NCAPH2, CHD1, FOS, MED1, TEAD3, MYB, SMAD1, MAFK, BCL11A, POU2F3, PCGF2, TCF3, BCOR, FOXP1, AATF, SMC3, STAG1, PAX7, TRP47, CBFA2T2, MEF2B, ZNF207, TBL1X, EBF1, WT1, KDM1A, YY1, RELA, TARDBP, JUNB, BRG1, SP140, ZIC2, HIF1A, GATA3, BATF, TAL1, MAX, ZNF143, NCOA3, NR2F2, NEUROG2, NR2F1, TP53, PKNOX1, MYOD1, T, ARRB1, AR, TAF1, RXR, HEXIM1, TFIIIC, ZBTB26, HSF1, BRD4, MAZ, AHR
  • Target gene symbol (double-evidenced CRMs): DNMT3L,HSF2BP,TSPEAR
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 51
  • Number of somatic mutations (non-coding): 17
  • Related genes and loops

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