Deatailed information for cohesin site CDBP00413558


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00413558
  • Locus: chr21-15682026-15683675
  • Data sourse: GSE126755, ENCSR000BTU, ENCSR230ZWH, GSE72082, GSE98367, GSE138405, GSE206145, GSE101921, ENCSR054FKH, GSE206145-NatGen2015, GSE120943, ENCSR000EDE, GSE68388, GSE103477, GSE111537, GSE108869, ENCSR000EDW, ENCSR000ECS, ENCSR917QNE
  • Cell type: MDM, Macrophage, RPE, Hela-Kyoto, Fibroblast, Monocytes, Hep-G2, Ishikawa, HCAEC, OCI-AML-3, HeLa-S3, Liver, Neutrophil, HuCC-T1
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 8% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.844
  • Subunit: SA1,Rad21,SMC1,SA2,Mau2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intergenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: False Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 56% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 66%, "7_Enh": 21%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, PGR, HMG20A, FOXA1, HLF, RXRB, ATF3, NFIC, MECOM, INTS11, JMJD1C, TEAD1, TRIM28, ELF1, KLF6, ETV1, RCOR2, LMO2, ESR1, HNF1B, USF2, CTCF, JUN, TCF12, EP300, BAF155, SOX5, SOX4, TRIM24, E2F1, SMC1, TEAD4, FOXA3, KMT2B, GATAD2A, CHD8, BRD3, DUX4, STAT1, GATAD1, SAP130, ARID3A, TBP, ERG, HOXC5, PAX6, ETS1, MYC, MCM5, SMARCA4, KDM4A, HOMEZ, RAD21, LHX2, GRHL3, RXRA, NKX2-1, GABPA, STAT3, ZNF614, XRCC5, NKX3-1, NFE2, VDR, NR3C1, CEBPB, STAT5B, KMT2A, CREB1, GABPB1, SPI1, MIXL1, TFE3, EHF, IRF1, INTS13, GATA2, ZNF644, FLI1, ZGPAT, MRTFB, NFIL3, ETV5, RUNX1, THAP11, SMC1A, BCL6, CEBPA, NKX2-2, SMAD3, SMARCC1, MYBL2, RARA, PRPF4, RUNX2, PBX4, ARNT, HMGB2, FOXM1, MAFB, ZNF10, FOS, CDK8, MED1, TEAD3, ZEB1, CEBPD, MYB, SMAD1, ZNF3, SETDB1, EVI1, SP1, BCL11A, NR4A1, HNF4A, IKZF5, TCF3, FOXP1, MLLT1, ETV4, SKI, PPARG, FOXA2, MEIS1, NFATC1, MIER2, MEF2C, CDK9, ZNF580, HOXB13, KDM1A, YY1, RELA, JUNB, AHR, GATA3, TAL1, MAX, ZNF143, KLF4, CEBPG, TCF7L2, TP53, NFKB1, MYOD1, ELF3, BRD2, KAT8, BHLHE40, AR, ZBTB16, ZBTB40, RXR, RNF2, BRD4, JUND, DMAP1, FOSL2
  • Target gene symbol (double-evidenced CRMs): USP25
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 8
  • Related genes and loops

eachgene