Deatailed information for cohesin site CDBP00417767


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  • Basic information
  • CohesinDB ID: CDBP00417767
  • Locus: chr21-34570400-34570594
  • Data sourse: GSE111537, GSE98367
  • Cell type: OCI-AML-3, Macrophage
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 0% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.978
  • Subunit: SA2,SMC1
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 93% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 55%, "5_TxWk": 31%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: PGR, SOX2, XBP1, FOXA1, SUZ12, LYL1, ATF3, NFIC, CHD7, RUNX3, PAX5, ZNF736, JMJD1C, TEAD1, TRIM28, LMO2, ESR1, MLL, TP73, USF2, JUN, CTCF, BAF155, KLF1, PAX8, DPF2, TRIM24, TEAD4, KMT2B, TFAP2C, EED, POU2F2, CHD8, MYCN, ZNF263, TOP2A, RUNX1T1, CTBP1, MTA2, ZBTB48, ZSCAN5A, STAT1, ZNF205, ZNF134, DDX5, ERG2, ERG, OGG1, MYC, SMARCA4, RAD21, GABPA, STAT3, NKX3-1, RCOR1, VDR, NR3C1, CEBPB, KMT2A, CREB1, EZH2, GRHL2, TRPS1, SPI1, HDAC2, GATA2, INTS13, ZNF766, NCOA2, RUNX1, BCL6, SMC1A, CEBPA, LDB1, SIN3A, ZFX, SMAD3, CREBBP, ZNF384, RUNX2, CDK6, PBX4, ARNT, ZNF10, FOS, CDK8, MED1, ZEB1, TERF1, TEAD3, ZNF558, SCRT2, PIAS1, MYB, TBX5, EVI1, STAT5A, BCL11A, SP1, HOXA9, CTBP2, FOXP1, SMC3, STAG1, MLLT1, FOXA2, MTA3, EBF1, MEIS1, WT1, ZBTB33, MEF2C, CDK9, HOXB13, RELA, JUNB, AHR, SP140, ZFP36, HIF1A, GATA3, TAL1, MAX, GATA1, ZNF143, TLE3, NCOA3, NR2F2, TCF7L2, KDM5B, TP53, ZNF334, AR, ZNF579, BRD4, SCRT1, MAZ, ZNF316
  • Target gene symbol (double-evidenced CRMs): RCAN1,SMIM11A,RUNX1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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