Deatailed information for cohesin site CDBP00416760


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  • Basic information
  • CohesinDB ID: CDBP00416760
  • Locus: chr21-31890447-31891698
  • Data sourse: ENCSR230ZWH, GSE72082, ENCSR501LQA, GSE165895, ENCSR000EFJ, GSE67783, GSE138405, GSE206145-NatGen2015, ENCSR806UKK, GSE135093, ENCSR895JMI, ENCSR193NSH, ENCSR768DOX, ENCSR981FDC, ENCSR807WAC, ENCSR620NWG, ENCSR853VWZ, ENCSR956LGB, ENCSR944ZCT, ENCSR054FKH, ENCSR537EFT, GSE126990, ENCSR748MVX
  • Cell type: Fibroblast, Hela-Kyoto, Hep-G2, A-549, IMR-90, Liver, HSPC, HFFc6
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 5% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.911
  • Subunit: SA1,Rad21,SMC1,SA2,Mau2,SMC3
  • 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: True ChIA-PET loops: True
  • Compartment: 71% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 40%, "5_TxWk": 24%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, PGR, HMG20A, FOXA1, HLF, INSM2, ATF3, PRDM1, ZNF189, MZF1, ZNF629, TEAD1, ETV1, ESR1, JUN, TCF12, EP300, BAF155, MNT, RFX5, FOXA3, GATAD2A, ZSCAN21, SAP130, TBP, ERG, OGG1, SMARCA4, RFX1, TSHZ1, RAD21, GRHL3, NKX2-1, STAT3, NKX3-1, RCOR1, ZNF639, NR3C1, CEBPB, EZH2, KLF8, GATA2, MXI1, NFIL3, BCL6, CEBPA, EZH2phosphoT487, SIN3A, SOX13, SMAD3, SMARCC1, PRDM10, ZNF35, ZNF184, PBX4, ZEB2, PBX3, FOS, SCRT2, PIAS1, MAFK, HNF4A, ARID1A, POU2F3, PHIP, FOXP1, PRDM6, ZNF394, FOXA2, SS18, ZNF600, ZNF692, ZSCAN16, ZNF574, HOXB13, KDM1A, RELA, JUNB, BRG1, GATA3, MAX, TLE3, CEBPG, SP7, TP53, NFKB1, BHLHE40, AR, ZNF366, BRD4, JUND, MAZ, FOSL2
  • Target gene symbol (double-evidenced CRMs): HUNK,MIS18A
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 3
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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