Deatailed information for cohesin site CDBP00416079


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  • Basic information
  • CohesinDB ID: CDBP00416079
  • Locus: chr21-28959314-28959751
  • Data sourse: GSE138405, GSE206145-NatGen2015, GSE165895
  • Cell type: Hela-Kyoto, Fibroblast, HFFc6
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 1% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.967
  • Subunit: Mau2,SA1,SA2,SMC1
  • 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: 68% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "5_TxWk": 50%, "4_Tx": 36%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, PGR, ZNF660, SOX2, MEIS2, FOXA1, RBFOX2, PBX2, MLL4, HNRNPK, ZNF90, ATF3, NFIC, CHD7, PRDM1, ZNF189, TEAD1, ZNF573, NFE2L2, ESR1, HNF1B, CTCF, TCF12, JUN, BAF155, EP300, SOX4, TEAD4, PDX1, NANOG, TOP2A, DUX4, TBP, HNF4G, ERG, MYC, ONECUT1, SMARCA4, GRHL3, PROX1, RXRA, GABPA, STAT3, NKX3-1, RCOR1, ZNF639, VDR, NR3C1, CEBPB, ESRRA, CREB1, EZH2, GRHL2, ZHX2, SPI1, HDAC2, GATA2, FLI1, MRTFB, RUNX1, MAFG, NKX2-2, SIN3A, SMAD3, PRDM10, CREBBP, ZNF384, RUNX2, GATA4, ZNF184, PBX4, SOX11, PBX3, MAFB, ZNF10, SUPT5H, FOS, MED1, CEBPD, SCRT2, PIAS1, NUP98-HOXA9, MAFK, RBM22, ARID1A, ASH2L, HOXA9, CTBP2, BCOR, FOXP1, PRDM6, FOXA2, GTF2B, WT1, FOXF1, ZBTB33, HOXB13, RELA, JUNB, BRG1, GATA3, TAL1, GATA1, AGO2, TLE3, SP7, TCF7L2, TP53, PHOX2B, T, BHLHE40, AR, ZBTB40, ZNF366, BRD4, SCRT1, JUND, ZZZ3, ZNF316, FOSL2
  • Target gene symbol (double-evidenced CRMs): LTN1,MAP3K7CL,USP16,CCT8
  • Function elements
  • Human SNPs: Initial_pursuit_acceleration_in_psychotic_disorders
  • Number of somatic mutations (coding): 105
  • Number of somatic mutations (non-coding): 35
  • Related genes and loops

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