Deatailed information for cohesin site CDBP00418911


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00418911
  • Locus: chr21-37538100-37538700
  • Data sourse: GSE116344, ENCSR153HNT
  • Cell type: K-562, RH4
  • 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): 0.978
  • Subunit: SA1,Rad21
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intergenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: non-Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 95% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 71%, "14_ReprPCWk": 22%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, NFIA, FOSL1, CBX5, SOX2, SUZ12, ATF3, NFIC, ZNF362, PRDM1, ATF4, SMARCE1, TP63, ELF1, TRIM28, TEAD1, TP73, CTCF, EP300, E4F1, MNT, DPF2, TRIM24, SOX6, TEAD4, TFAP2C, GLIS1, CHD8, ZSCAN5D, POU5F1, MYCN, TOP2A, ID3, CTBP1, ZBTB48, ZSCAN5A, DUX4, HINFP, ZNF205, SRF, MYC, SMARCA4, ARID1B, ZNF398, IKZF1, RCOR1, LEF1, NR2F6, NR3C1, CEBPB, ESRRA, ZNF652, HES1, SPI1, HDAC2, GATA2, ZNF644, SMARCA5, EP400, ATF1, CC2D1A, RUNX1, CBX1, HDAC1, CEBPA, SOX13, ZNF534, ZFX, TET2, PRDM10, MYBL2, ZNF384, GATA4, OSR2, NRF1, HMBOX1, SMAD4, FOXM1, CBFA2T3, NR2C1, CDK8, MED1, TEAD3, ZMYM3, VEZF1, TAF7, NCOA1, L3MBTL2, SETDB1, TBX5, SP1, NR4A1, REST, ZBTB7A, RBM25, ATF7, ASH2L, AFF1, BCOR, AATF, SMC3, MLLT1, STAG1, PTTG1, CBX3, MTA3, CREM, RBBP5, WT1, KDM1A, YY1, RELA, ZNF148, SP140, ZFP36, SKIL, ZIC2, ZNF519, TAL1, MAX, GATA1, GFI1B, NR2F2, NCOA3, NR2F1, KDM5B, TP53, TAF1, ZBTB40, NCOR1, RNF2, JUND, ILF3, BRD4, MAZ, IRF9, MEF2D
  • Target gene symbol (double-evidenced CRMs): DYRK1A,KCNJ6,VPS26C,TTC3
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 1
  • Related genes and loops

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