Deatailed information for cohesin site CDBP00416530


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  • Basic information
  • CohesinDB ID: CDBP00416530
  • Locus: chr21-31298480-31299818
  • Data sourse: ENCSR000EAC, ENCSR000DZP, ENCSR230ZWH, GSE86191, GSE98367, GSE206145, GSE120943, GSE50893, ENCSR917QNE
  • Cell type: HCT-116, Monocytes, GM12878, GM2588, Liver, Macrophage, B-cell
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 2% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.922
  • Subunit: SA1,Rad21,SMC1,Mau2,SMC3
  • CTCF binding site: non-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: 59% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 70%, "7_Enh": 14%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: NME2, XBP1, HNF1A, FOXA1, HDGF, PRDM1, PAX5, ZSCAN4, TP63, ZNF467, ZNF629, MAF, KLF6, ESR1, HNF1B, TP73, OCA2, CTCF, EP300, DPF2, RAD51, PDX1, POU2F2, CHD8, MTA2, DUX4, NBN, ARID3A, ZNF300, ZBTB21, MYC, ONECUT1, RAD21, GRHL3, RXRA, NKX3-1, IKZF1, RCOR1, ZNF639, ARNTL, ZNF750, NR3C1, CEBPB, CREB1, EZH2, KLF8, SPI1, IRF1, GATA2, SMARCA5, RELB, SMC1A, CEBPA, NKX2-2, SOX13, ZFX, TRIM22, PRDM10, ZNF35, ARNT, ATF2, PBX3, MAFB, CDK8, MED1, CEBPD, MYB, SMAD1, KLF9, BCL11A, SP1, HNF4A, ATF7, ASH2L, NCOR2, MLLT1, NFATC3, MEF2B, FOXA2, ZNF207, EBF1, E2F8, ZNF692, ZNF823, HOXB13, KDM1A, YY1, RELA, TARDBP, ZFP36, SKIL, HIF1A, BATF, TAL1, ZNF143, KLF4, NCOA3, ZNF791, KDM5B, TP53, PKNOX1, ZNF687, ELF3, TBX21, BHLHE40, AR, PAX3-FOXO1, ZBTB40, ZNF366, IKZF2, BRD4, MAZ, ZSCAN23
  • Target gene symbol (double-evidenced CRMs): TIAM1,EVA1C
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 30
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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