Deatailed information for cohesin site CDBP00419370


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  • Basic information
  • CohesinDB ID: CDBP00419370
  • Locus: chr21-39033437-39035154
  • Data sourse: ENCSR230ZWH, GSE72082, ENCSR000BSB, GSE25021, ENCSR000EDW, ENCSR917QNE, GSE67783, GSE86191, GSE76893, GSE206145-NatGen2015, ENCSR000EEG, ENCSR338DUC, GSE98367, ENCSR000BLS, GSE206145, ENCSR635OSG, ENCSR167MTG, GSE111913, ENCSR054FKH, ENCSR153HNT, GSE68388
  • Cell type: RPE, Macrophage, Fibroblast, HCT-116, Hep-G2, RT-112, K-562, Liver, HSPC, HuCC-T1
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 8% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.889
  • Subunit: NIPBL,SA1,Rad21,SMC1,SA2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: TSS,TES,Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 96% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 34%, "7_Enh": 23%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: NFIA, PGR, HMG20A, ZNF660, HNF1A, XBP1, FOXA1, SUZ12, RBFOX2, RXRB, PBX2, MLL4, KDM3A, TFAP4, TSC22D4, ZNF90, THRB, ATF3, NFIC, ZFP64, THAP1, CTCFL, PRDM1, CBFB, MXD4, TP63, MITF, MAF, JMJD1C, TEAD1, ELF1, KLF6, RBM39, ETV1, KLF10, RCOR2, ESR1, OCA2, USF2, CTCF, TCF12, JUN, EP300, MNT, SOX9, SOX5, DPF2, DMAP1, E2F6, RFX5, RFX3, SMC1, TEAD4, FOXA3, ZNF175, GATAD2A, RBPJ, TFAP2C, MLX, GLIS1, POU2F2, ZSCAN5D, MYCN, HHEX, CDK7, POU5F1, RUNX1T1, CTBP1, KDM4C, DUX4, ZBTB48, STAT1, ZSCAN5A, SRF, GATAD1, SAP130, GMEB2, ARID3A, TBP, HNF4G, ERG, PBX1, OGG1, ETS1, MYC, EZH1, SMARCA4, ONECUT1, HOMEZ, RAD21, GRHL3, RXRA, NKX2-1, FOXK2, MCRS1, GABPA, STAT3, ZNF614, XRCC5, PRDM14, IKZF1, MIER3, RCOR1, NR2F6, HNRNPH1, CEBPB, SRSF3, HNRNPL, KMT2A, CREB1, CCAR2, TBL1XR1, EZH2, GRHL2, ZNF652, GABPB1, ZHX2, HES1, TFE3, MIXL1, HBP1, ZSCAN2, EHF, HDAC2, SSRP1, ZNF644, GATAD2B, MXD3, FLI1, DRAP1, ZGPAT, MXI1, HCFC1, SMARCA5, NFIL3, ATF1, ETV5, PTBP1, RUNX1, THAP11, CTNNB1, BCL6, CBX1, CEBPA, SMC1A, SIRT6, SOX13, ZFX, SIN3A, FIP1L1, SMAD3, TET2, CBX8, TBX3, SP5, ERG3, SMARCC1, MYBL2, RARA, PRPF4, NOTCH1, IRF2, ZNF384, NFYC, ZBTB2, GATA4, ARNT, ZNF48, SMAD4, FOS, HMGXB4, SMARCB1, TGIF2, MED1, TEAD3, ZEB1, CEBPD, U2AF1, ZMYM3, ZNF3, NR1H2, KLF9, L3MBTL2, TBX5, MBD1, SETDB1, RBM22, USF1, SP1, TFAP2A, NIPBL, HNF4A, NR4A1, BCL11A, IKZF5, REST, ZBTB7A, RBM25, ASH2L, HNRNPLL, ZNF605, TCF3, FOXP1, BCOR, AATF, SMC3, STAG1, ETV4, SKI, TRP47, CBFA2T2, PPARG, FOXA2, AGO1, EBF1, CREM, MEIS1, TBL1X, MIER2, CBX3, MTA3, WT1, MAFF, ZBTB33, TCF7, ZNF580, ZKSCAN1, FOXO3, KDM1A, YY1, RELA, JUNB, SP140, ZFP36, HIF1A, MGA, TAL1, MAX, GATA1, ZNF143, CBX2, CEBPG, NCOA3, NR2F2, NR2F1, ZNF768, TP53, RUVBL1, PHOX2B, PHF5A, ELF3, KAT8, BRD2, ARID4B, NFKBIZ, BHLHE40, TAF1, AR, RXR, EGLN2, EGR1, HEXIM1, RB1, HSF1, ZBTB26, RNF2, BRD4, JUND, NCOR1, CLOCK, CUX1, MAZ, SMAD4.1D12, TBX2, ZNF24, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): ETS2
  • Function elements
  • Human SNPs: Glaucoma_(primary_open-angle)
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 6
  • Related genes and loops

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