Deatailed information for cohesin site CDBP00419006


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00419006
  • Locus: chr21-37817250-37818781
  • Data sourse: ENCSR000EFJ, GSE98367, GSE138405, ENCSR404BPV, GSE206145, GSE206145-NatGen2015, GSE135093, GSE120943, ENCSR198ZYJ, GSE165895
  • Cell type: RPE, Hela-Kyoto, Fibroblast, Monocytes, Neurons-H1, IMR-90, Macrophage, HFFc6
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 4% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.911
  • Subunit: Rad21,SMC1,SA2,Mau2,SMC3
  • CTCF binding site: non-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): True
  • Chromatin annotation: "15_Quies": 52%, "7_Enh": 22%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: PGR, ZNF697, SOX2, XBP1, FOXA1, CHD7, PRDM1, PAX5, ZSCAN4, ZNF506, TEAD1, TRIM28, ESR1, OCA2, CTCF, TCF12, EP300, PAX8, PDX1, POU2F2, CHD8, NANOG, ZNF263, MYCN, POU5F1, KDM4C, TOP2A, ZBTB48, ZSCAN5A, STAT1, DDX5, TBP, ERG, MYC, RAD21, GRHL3, GABPA, STAT3, RCOR1, NR3C1, EZH2, ZHX2, SPI1, HDAC2, SIX2, FLI1, SMARCA5, ZNF490, RUNX1, SMC1A, NKX2-2, EZH2phosphoT487, AFF4, ZFX, POU4F2, CBX8, ZNF384, NOTCH1, BRD9, RUNX2, CDK6, NRF1, ARNT, PRDM9, MAFB, MED1, TERF1, MYB, ZMYM3, USF1, REST, RBM25, BCOR, FOXP1, SMC3, STAG1, PPARG, FOXA2, WT1, MEF2C, HOXB13, KDM1A, YY1, RELA, SP140, ZFP36, HIF1A, GATA3, ZNF143, GATA1, CBX2, NR2F1, ZNF768, NEUROG2, TP53, ZNF334, MYOD1, BHLHE40, AR, YAP1, NOTCH3, BRD4, MAZ, ADNP, AHR
  • Target gene symbol (double-evidenced CRMs): ERG,KCNJ6
  • Function elements
  • Human SNPs: Smoking_initiation_(ever_regular_vs_never_regular)_(MTAG)
  • Number of somatic mutations (coding): 30
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

eachgene