Deatailed information for cohesin site CDBP00418056


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  • Basic information
  • CohesinDB ID: CDBP00418056
  • Locus: chr21-35336854-35337807
  • Data sourse: ENCSR000BLD, GSE72082, ENCSR000BSB, ENCSR000BLY, GSE105028, GSE25021, GSE131606, GSE67783, ENCSR000BKV, GSE86191, GSE101921, GSE120943, GSE116344, GSE94872, ENCSR000BLS, GSE206145, ENCSR000ECE, GSE97394, ENCSR167MTG, GSE129526, ENCSR054FKH, ENCSR153HNT, GSE83726, GSE50893
  • Cell type: RPE, H1-hESC, HCT-116, Monocytes, Hep-G2, RH4, GM19240, HUVEC, HCAEC, DKO, GM12890, HUES64, SK-N-SH, K-562, HSPC, H9-hESC
  • 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): 0.822
  • Subunit: SA1,Rad21,SA2,SMC1
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intergenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 81% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 76%, "14_ReprPCWk": 16%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, MEIS2, PBX2, ATF3, NFIC, THAP1, SMARCE1, MAF, TRIM28, NFE2L2, ESR1, CTCF, TCF12, JUN, EP300, DPF2, TRIM24, SOX6, DDX20, SMC1, TEAD4, ZNF317, MTA2, DUX4, STAT1, ARID3A, ERG, SMARCA4, ARID1B, RAD21, GRHL3, NKX2-1, GABPA, STAT3, NFE2, RCOR1, CEBPB, HDAC2, GATA2, NCOA2, ZIM3, MAFG, CEBPA, LDB1, ZFX, SMAD3, ZBTB2, RUNX2, GATA4, ARNT, ZEB2, CBFA2T3, FOS, MED1, GMEB1, PML, CEBPD, C11orf30, STAT5A, KLF16, MAFK, BCL11A, REST, STAG2, STAG1, CBFA2T2, CBX3, MTA3, CREM, FOXA2, MAFF, WT1, ZBTB33, RELA, JUNB, HIF1A, TAL1, MAX, GATA1, CEBPG, NCOA3, NR2F2, NR2F1, PKNOX1, ZNF334, MYOD1, AR, MYNN, RNF2, NCOR1, BRD4, JUND, ZNF316
  • Target gene symbol (double-evidenced CRMs): SMIM11A
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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