Deatailed information for cohesin site CDBP00421061


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  • Basic information
  • CohesinDB ID: CDBP00421061
  • Locus: chr21-44652956-44653464
  • Data sourse: GSE67783, GSE86191, GSE72082, GSE111913, ENCSR054FKH
  • Cell type: RT-112, HCT-116, HSPC, Hep-G2
  • 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): 0.956
  • Subunit: SA1,Rad21,SMC1
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: TSS,TES
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 80% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 48%, "14_ReprPCWk": 32%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, NFIA, ZNF496, HMG20A, PBX2, RXRB, KDM3A, ZNF90, ATF3, CBFB, MXD4, MITF, TEAD1, KLF6, SNAI2, LMO2, ESR1, CTCF, JUN, TCF12, MNT, SOX5, E2F6, E2F4, TEAD4, FOXA3, ZNF175, GATAD2A, GTF2F1, TFAP2C, MLX, GLIS1, POU2F2, MYCN, POU5F1, CTBP1, ZBTB48, GATAD1, SAP130, PBX1, ASCL1, OGG1, MYC, SMARCA4, HOMEZ, GRHL3, GABPA, STAT3, PRDM14, MIER3, DNMT3B, NR2F6, STAT5B, CREB1, EZH2, GABPB1, TFE3, MXD3, FLI1, NR2C2, ETV5, RUNX1, THAP11, CBX1, SMC1A, CEBPA, EZH2phosphoT487, SOX13, ZFX, ERG3, RARA, ARNT, TFDP1, ZNF48, SMAD4, NR2C1, CHD1, TEAD3, MYB, L3MBTL2, SETDB1, USF1, SP1, REST, TCF3, AATF, SMC3, STAG1, NFATC3, TRP47, CBX3, FOXA2, E2F8, WT1, CDK9, ZNF580, YY1, RELA, SP140, ZIC2, HIF1A, MGA, TAL1, MAX, MAF1, NR2F1, TP53, MYOD1, ELF3, KAT8, TBX21, BHLHE40, NFKBIZ, RXR, ZBTB42, HEXIM1, ZBTB26, RNF2, HSF1, BRD4, JUND, CLOCK, MAZ, AHR
  • Target gene symbol (double-evidenced CRMs): ADARB1,ITGB2,TSPEAR,PTTG1IP
  • Function elements
  • Human SNPs: 3-month_functional_outcome_in_ischaemic_stroke_(modified_Rankin_score)
  • Number of somatic mutations (coding): 18
  • Number of somatic mutations (non-coding): 6
  • Related genes and loops

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