Deatailed information for cohesin site CDBP00416770


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  • Basic information
  • CohesinDB ID: CDBP00416770
  • Locus: chr21-31911007-31912130
  • Data sourse: GSE67783, GSE86191, GSE138405, GSE206145-NatGen2015, GSE126990, GSE165895
  • Cell type: Hela-Kyoto, Fibroblast, HCT-116, HSPC, HFFc6
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 3% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.944
  • Subunit: SA1,Rad21,SMC1,SA2,Mau2
  • CTCF binding site: 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: 71% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 36%, "14_ReprPCWk": 21%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, FOSL1, PGR, ZNF660, XBP1, PATZ1, FOXA1, LEO1, MLL4, ZFHX2, THRB, ATF3, CHD7, KLF14, ZNF629, MYOG, TEAD1, TRIM28, NFE2L2, ESR1, OCA2, JUN, CTCF, KLF1, PAX8, E2F1, TEAD4, TFAP2C, GLIS1, CHD8, BRD1, ZSCAN5D, MYCN, ZNF263, POU5F1, CTBP1, ZSCAN21, ZBTB17, ZBTB48, ZSCAN5A, ERG2, ZBTB21, SMARCA4, TSHZ1, RAD21, GRHL3, NKX2-1, APC, XRCC5, STAT3, RCOR1, ZNF639, ZNF750, NR3C1, CEBPB, CREB1, EZH2, KLF17, GATA2, MXD3, SIX2, PTBP1, RUNX1, ZNF335, ZFX, SIN3A, AFF4, SMAD3, ZNF214, TET2, ERG3, SMARCC1, PRDM10, TWIST1, ZNF18, ZNF133, CDK6, OSR2, ZNF184, PBX4, ARNT, ZNF48, PRDM9, SMAD4, SP2, FOS, SCRT2, ZBTB18, NCOA1, TBX5, RBM22, MAFK, BCL11A, TFAP2A, SP1, ARID2, NKX2-5, ZNF479, HNRNPLL, SMC3, ELL2, STAG1, CBFA2T2, FOXA2, SS18, ZNF600, ZNF692, WT1, YY1, RELA, JUNB, BRG1, ISL1, SP140, ZIC2, MTA1, AGO2, HAND2, ZFP69B, SP7, NR2F1, TP53, MYOD1, EGR2, BRD2, BHLHE40, AR, ZBTB42, ZNF366, ZBTB26, HSF1, BRD4, SCRT1, CLOCK, MAZ, TBX2, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): HUNK
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 6
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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