Deatailed information for cohesin site CDBP00418642


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  • Basic information
  • CohesinDB ID: CDBP00418642
  • Locus: chr21-36891744-36892476
  • Data sourse: GSE206145, GSE206145-NatGen2015, GSE73207
  • Cell type: RPE, TF-1, Fibroblast
  • 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,SMC3,Rad21
  • 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: 94% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "5_TxWk": 55%, "15_Quies": 23%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: CBFA2T2, ZNF554, CHD8, FOXA2, MYCN, LDB1, MEIS1, POU5F1, ZFX, ZNF600, XBP1, DUX4, WT1, STAT1, ZBTB48, ZSCAN5A, SRF, SMC1A, PBX2, TWIST1, ZNF549, ERG, YY1, RELA, ZBTB8A, NEUROD1, RUNX2, GATA4, OSR2, ISL1, SP140, ARNT, ZIC2, ZNF189, GRHL3, OTX2, GATA3, SMC3, HMBOX1, ZEB2, APC, CBFA2T3, MAX, TAL1, GATA1, STAT3, MITF, RCOR1, HAND2, NFE2, ZNF736, ZFP69B, SP7, GFI1B, TRIM28, SCRT2, ESR1, EBF3, PHOX2B, CTCF, RBM22, USF1, TCF12, BCL11A, AR, HDAC2, GATA2, ZBTB7A, ZBTB42, FLI1, RAD51, GABPA, BRD4, SCRT1, ZNF350, MRTFB, TEAD4, TBX2, ZNF24, ZNF316
  • Target gene symbol (double-evidenced CRMs): HLCS
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 6
  • Number of somatic mutations (non-coding): 2
  • Related genes and loops

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