Deatailed information for cohesin site CDBP00417900


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  • Basic information
  • CohesinDB ID: CDBP00417900
  • Locus: chr21-34928415-34928925
  • Data sourse: GSE67783, GSE86191, ENCSR000BLY, GSE206145, ENCSR000EHX
  • Cell type: RPE, HCT-116, HSPC, SK-N-SH
  • 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
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: False Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 91% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 50%, "5_TxWk": 29%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, NFIA, HMG20A, RXRB, UBTF, PBX2, KDM3A, ATF3, NFIC, RUNX3, PRDM1, ATF4, CBFB, CDX2, TEAD1, ZNF121, TRIM28, NFE2L2, RCOR2, TP73, CTCF, TCF12, EP300, SOX5, PAX8, DMAP1, IRF4, TEAD4, FOXA3, ZNF175, GATAD2A, RBPJ, DUX4, STAT1, MLLT3, DDX5, SAP130, TBP, HNF4G, SMARCA4, HOMEZ, RAD21, GRHL3, RXRA, PROX1, NKX2-1, BATF3, XRCC5, ZNF614, IKZF1, RCOR1, NFE2, NR2F6, CEBPB, KMT2A, EZH2, GRHL2, ZNF652, GABPB1, ZNF436, SPI1, MIXL1, ZNF257, HDAC2, GATA2, ZNF644, DRAP1, ZGPAT, ZNF766, NFIL3, ETV5, RUNX1, THAP11, MAFG, BCL6, CEBPA, NKX2-2, SOX13, ZFX, PRDM10, RARA, ZNF384, RUNX2, GATA4, DAXX, BACH1, NRF1, ZNF48, SMAD4, HMBOX1, PBX3, MAFB, SUPT5H, CDK8, MED1, TEAD3, NR1H2, C11orf30, MAFK, SP1, BCL11A, NR4A1, HNF4A, REST, POU2F3, ASH2L, PHIP, STAG1, PPARG, FOXA2, MIER2, MAFF, ZBTB33, MEF2C, ZNF580, KDM1A, RELA, AHR, HIF1A, GATA3, BATF, MAX, ZNF143, GATA1, HAND2, CEBPG, GFI1B, NR2F2, TP53, MED, ZNF334, PHOX2B, ELF3, BRD2, KAT8, ARID4B, AR, NFKBIZ, NCOR1, JUND, BRD4, ZNF316, FOSL2
  • Target gene symbol (double-evidenced CRMs): RUNX1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 8
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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