Deatailed information for cohesin site CDBP00419536


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  • Basic information
  • CohesinDB ID: CDBP00419536
  • Locus: chr21-39565337-39565914
  • Data sourse: GSE120943, GSE67783, GSE98367
  • Cell type: Monocytes, HSPC, Macrophage
  • 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): 0.967
  • Subunit: SA1,SMC1
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 69% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 60%, "14_ReprPCWk": 32%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: PGR, SOX2, NME2, XBP1, FOXA1, SUZ12, PBX2, ZNF28, ZBTB7B, HDGF, ATF3, NFIC, CHD7, PRDM1, ZNF444, DPF1, ZSCAN4, MITF, ZNF320, ZNF467, TEAD1, BCLAF1, ZNF217, ESR1, PITX3, ZIK1, CTCF, JUN, TCF12, EP300, E4F1, BAF155, DPF2, E2F6, IRF4, RFX5, ZNF512B, ZNF776, E2F1, ZNF350, TEAD4, PDX1, TFAP2C, EHMT2, GLIS1, NANOG, RUNX1T1, CTBP1, ZBTB48, STAT1, NONO, ERG, PBX1, ASCL1, MYC, RFX1, RAD21, GRHL3, NKX2-1, GABPA, STAT3, NKX3-1, ZNF398, IKZF1, RCOR1, HNRNPH1, DACH1, VDR, NR3C1, CEBPB, CREB1, EZH2, GRHL2, EBF3, TRPS1, SPI1, HDAC2, GATA2, GATAD2B, RUNX1, CBX1, SMC1A, NKX2-2, SIN3A, ZFX, PCBP2, ERG3, CREBBP, ZNF384, RUNX2, ARNT, NFIB, FOS, MED1, PIAS1, KLF9, USF1, SP1, TFAP2A, POU2F3, ASH2L, CTBP2, TCF3, FOXP1, SMC3, STAG1, FOXA2, CHD2, WT1, ZNF662, HOXB13, ZKSCAN1, RELA, NEUROD1, ZNF148, MCM3, HIF1A, OTX2, GATA3, TAL1, MAX, NRIP1, GATA1, MTA1, TCF7L2, KDM5B, TP53, PKNOX1, ZNF687, MYOD1, EGR2, AR, PAX3-FOXO1, EGLN2, ZNF366, EGR1, HSF1, NCOR1, BRD4, SCRT1, CUX1, MAZ, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): B3GALT5
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 3
  • Number of somatic mutations (non-coding): 3
  • Related genes and loops

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