Deatailed information for cohesin site CDBP00416980


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  • Basic information
  • CohesinDB ID: CDBP00416980
  • Locus: chr21-32473670-32479773
  • Data sourse: ShirahigeLab-GSE177045, ENCSR000BSB, ENCSR501LQA, GSE116868, ENCSR150EFU, GSE131606, ENCSR330ELC, ENCSR917QNE, GSE165895, GSE67783, GSE86191, GSE138405, GSE101921, ShirahigeLab-NatGen2015, GSE94872, ShirahigeLab, ENCSR247LSH, ENCSR767DFK, ENCSR984DZW, ENCSR495WGO, ENCSR853VWZ, GSE110061, ENCSR000HPG, GSE111913, ENCSR335RKQ, ENCSR153HNT, GSE68388, GSE126990, ENCSR748MVX
  • Cell type: MCF-7, RPE, Fibroblast, HCT-116, Hela-Kyoto, MB157, A-549, HUVEC, HCAEC, RT-112, IMR-90, HSPC, K-562, Liver, HFFc6, HuCC-T1, DKO
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 14% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.811
  • Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 90% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "5_TxWk": 35%, "7_Enh": 24%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, NANOG, FOXA2, SOX2, ZFX, STAG2, NME2, PAF1, SMAD3, WT1, ZSCAN5A, FOXA1, MLL4, SMARCC1, HOXC5, ERG, RELA, IRF2, JUNB, ETS1, RUNX2, MYC, SMARCA4, NFIC, OSR2, RAD21, PBX4, DAXX, CBFB, HMGB2, OTX2, GLYR1, GATA3, APC, STAT3, MAX, TAL1, XRCC5, CDK8, MITF, UBN1, TP63, MED1, FOS, GATA1, KLF4, MAF, ZNF121, KMT2A, KLF6, ETV1, TCF7L2, MYB, TP53, ESR1, TP73, BMPR1A, ZIM3, HNF1B, GRHL2, JUN, CTCF, ELF3, BCL11A, TCF12, TBX21, AR, IRF1, GATA2, BRD4, PHIP, E2F1, MAZ, SMC1, SMC3, STAG1, TFAP2C, FOSL2
  • Target gene symbol (double-evidenced CRMs): IL10RB,CFAP298,AP000295.1,CFAP298-TCP10L,URB1,EVA1C,TIAM1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 156
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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