Deatailed information for cohesin site CDBP00418575


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  • Basic information
  • CohesinDB ID: CDBP00418575
  • Locus: chr21-36737205-36737911
  • Data sourse: GSE67783, GSE86191, GSE206145, GSE206145-NatGen2015, ENCSR153HNT
  • Cell type: RPE, Fibroblast, HCT-116, K-562, HSPC
  • 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): 0.944
  • Subunit: SA1,Rad21,SA2
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: non-Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 92% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "14_ReprPCWk": 54%, "15_Quies": 24%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: RUNX1, GLIS1, FOXO1, TRP47, POU2F2, BRD1, FOXA2, ZNF263, MYCN, SIRT6, PAF1, ZFX, KDM4C, MTA2, WT1, ZSCAN5A, ZBTB48, STAT1, TET2, ERG3, DDX5, ERG2, CDK9, ZFHX2, KDM1A, ERG, RELA, CREBBP, TARDBP, ATF3, MYC, SMARCA4, CTCFL, SP140, ZIC2, GRHL3, PRDM1, MAX, AGO2, VDR, CBX2, NR3C1, TRIM28, ZNF121, SCRT2, NEUROG2, NR2F1, KDM5B, ZNF512, RBM39, OCA2, ZNF334, ZSCAN22, ZNF37A, EGR2, SREBF2, CTCF, MYOD1, JUN, AR, SOX4, YAP1, ZBTB7A, EGLN2, ZNF366, RBM25, FLI1, HSF1, RNF2, SCRT1, BRD4, BCOR, MAZ, AATF, MYF5, STAG1, AHR
  • Target gene symbol (double-evidenced CRMs): HLCS,SIM2,TTC3
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 6
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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