Deatailed information for cohesin site CDBP00420562


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  • Basic information
  • CohesinDB ID: CDBP00420562
  • Locus: chr21-42987592-42989052
  • Data sourse: GSE206145-GSE177045, GSE67783, GSE86191, GSE206145, GSE206145-NatGen2015, ENCSR153HNT, GSE165895
  • Cell type: MCF-7, RPE, Fibroblast, HCT-116, K-562, HSPC, HFFc6
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 2% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.922
  • 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: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 83% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "5_TxWk": 66%, "15_Quies": 17%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, FOSL1, MEIS2, XBP1, TBL1X, PATZ1, FOXA1, PBX2, LEO1, TFAP4, HDGF, ATF3, ZFP64, ZNF362, THAP1, RUNX3, ATF4, MORC2, CBFB, ZNF189, SMARCE1, PAX5, MITF, ZNF629, ELF1, TRIM28, TEAD1, ETV1, NFE2L2, LMO2, ESR1, OCA2, SAP30, HDAC8, USF2, CTCF, TCF12, JUN, EP300, E4F1, MNT, GATA6, DPF2, PAX8, SOX4, E2F6, TRIM24, SOX6, DEK, E2F4, E2F1, ZNF528, ZNF350, SMC1, TEAD4, GATAD2A, GTF2F1, RBPJ, EED, GLIS1, POU2F2, CHD8, BRD1, ZSCAN5D, MYCN, POU5F1, BRD3, ID3, CTBP1, MTA2, ZBTB17, ZBTB48, ZSCAN21, ZSCAN5A, NONO, SRF, DDX5, NBN, ARID3A, ERG, ETS1, MYC, SMARCA4, ARID1B, RAD21, FOXP2, GRHL3, NKX2-1, FOXK2, GABPA, STAT3, IKZF1, RCOR1, NFE2, NR2F6, MIER3, ARNTL, DACH1, NR3C1, ESRRA, CEBPB, ZNF93, LEF1, SRSF3, KMT2A, CREB1, EZH2, GABPB1, ZHX2, SPI1, EHF, IRF1, HDAC2, GATA2, TAF9B, FLI1, MXI1, SMARCA5, MRTFB, NCOA2, ATF1, ETV5, PTBP1, RUNX1, BCL6, MAFG, HDAC1, CEBPA, LDB1, AFF4, ZFX, SIN3A, SMAD3, ZNF770, TET2, ZNF18, PRDM10, SMARCC1, ZNF384, NOTCH1, RUNX2, GATA4, ARNT, NRF1, PBX4, ATF2, HMGB2, HMBOX1, CBFA2T3, FOXM1, PBX3, FOS, CDK8, SMARCB1, SUPT5H, CHD1, MED1, CSNK2A1, TEAD3, PML, ZXDB, CEBPD, TERF1, SMAD1, SUPT16H, ZNF3, C11orf30, NCOA1, L3MBTL2, TBX5, KLF16, ZNF22, RBM22, USF1, BCL11A, MAFK, FOXA2, REST, ZBTB7A, ZNF479, CCNT2, ATF7, ZHX1, PHIP, BCOR, FOXP1, TCF3, AFF1, GLIS2, AATF, SMC3, MLLT1, STAG1, ZNF394, NFATC3, TRP47, CBFA2T2, PPARG, ZNF316, MTA3, CREM, MEIS1, PAF1, CHD2, ZNF600, ZSCAN16, RBBP5, WT1, MAFF, ZNF574, ZBTB33, HOXB13, MPHOSPH8, KDM1A, YY1, RELA, ZNF318, JUNB, NEUROD1, SP140, TCF4, SKIL, HIF1A, GATA3, TAL1, MAX, NRIP1, GATA1, AGO2, ZNF143, ZNF333, PLAG1, CEBPG, GFI1B, NR2F2, NCOA3, NR2F1, NEUROG2, KDM5B, TP53, ZBTB6, PKNOX1, MED, ZNF334, MYOD1, BRD2, BHLHE40, AR, ZBTB40, YAP1, ZNF324, MYNN, NCOR1, RNF2, BRD4, ILF3, ZBTB26, CLOCK, JUND, MAZ, HSF1, ZNF24, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): CFAP410,UBE2G2,TRPM2,PFKL,SUMO3,DNMT3L,RRP1B,PKNOX1,UMODL1,HSF2BP
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 14
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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