Deatailed information for cohesin site CDBP00421205


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  • Basic information
  • CohesinDB ID: CDBP00421205
  • Locus: chr21-45163388-45165275
  • Data sourse: GSE67783, GSE86191, GSE206145, GSE206145-NatGen2015, ENCSR153HNT, GSE83726
  • Cell type: RPE, Fibroblast, RH4, HCT-116, K-562, HSPC
  • 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): 0.933
  • Subunit: SA1,Rad21,SA2
  • 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: 85% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "5_TxWk": 47%, "15_Quies": 23%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, TRIM25, PGR, ZSCAN5C, XBP1, FOXA1, LEO1, ZFHX2, ATF3, NFIC, PAX5, TP63, MITF, MYOG, ELF1, TRIM28, SNAI2, ESR1, OCA2, USF2, CTCF, TCF12, BAF155, MNT, PAX8, TRIM24, E2F1, TEAD4, GLIS1, POU2F2, BRD1, MYCN, POU5F1, ZNF263, MTA2, DUX4, ZBTB48, ZSCAN5A, ERG2, ERG, PBX1, ASCL1, OGG1, MYC, SMARCA4, GRHL3, STAT3, XRCC5, NKX3-1, PRDM14, DNMT3B, NR3C1, KMT2A, CREB1, EZH2, BMPR1A, GRHL2, SPI1, GATA2, SIX2, FLI1, MYF5, RUNX1, BCL6, SIRT6, CRY1, SIN3A, ZFX, ZNF534, TET2, ERG3, TAF15, RUNX2, CHD1, ZNF264, SCRT2, PIAS1, ZNF680, ZNF3, TBX5, SREBF2, RBM22, USF1, NKX2-5, REST, ATF7, HOXA9, HNRNPLL, TCF3, BCOR, AATF, SMC3, NCOR2, STAG1, TRP47, MEF2B, FOXA2, EBF1, PAF1, ZNF600, WT1, HOXB13, YY1, RELA, TARDBP, JUNB, NEUROD1, SP140, ZFP36, TCF4, ZIC2, OTX2, MAF1, MAX, TAL1, AGO2, CBX2, TLE3, NEUROG2, NR2F1, KDM5B, TP53, PKNOX1, ZNF334, NFKB1, MYOD1, EGR2, TBX21, AR, EGR1, HEXIM1, HSF1, SCRT1, BRD4, MAZ
  • Target gene symbol (double-evidenced CRMs): PCBP3,POFUT2,ADARB1,COL18A1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 36
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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