Deatailed information for cohesin site CDBP00417499


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  • Basic information
  • CohesinDB ID: CDBP00417499
  • Locus: chr21-33819690-33821242
  • Data sourse: GSE67783, GSE86191, GSE126634, GSE111913, GSE206145, GSE152721, GSE206145-NatGen2015
  • Cell type: RPE, Fibroblast, HCT-116, HSPC, RT-112, HAP1
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 2% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.933
  • 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: False ChIA-PET loops: True
  • Compartment: 90% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "5_TxWk": 52%, "4_Tx": 22%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, NFIA, HMG20A, ZSCAN5C, SOX2, XBP1, FOXA1, PBX2, ZBTB44, ZNF322, IKZF3, PRDM1, CHD7, ZNF189, MITF, TRIM28, ESR1, OCA2, USF2, ZNF561, JUN, CTCF, TEAD4, KLF3, PDX1, RBPJ, TFAP2C, GLIS1, CHD8, ZNF263, TOP2A, ZNF778, ZNF317, ZBTB17, ZBTB48, SRF, SP4, HNF4G, OGG1, MYC, SMARCA4, GRHL3, XRCC5, SOX10, CEBPB, FEZF1, HDAC2, GATA2, ZNF644, CEBPA, ZNF335, ZFX, SOX13, ZBTB12, TET2, RARA, ZNF384, GATA4, OSR2, DAXX, ATF2, SMAD4, FOXM1, MED1, ZXDB, SCRT2, NUP98-HOXA9, RBM22, USF1, PHIP, PRDM6, SMC3, ELL2, PPARG, FOXA2, TBL1X, ZNF692, WT1, ESR2, YY1, RELA, ZIC2, HIF1A, GATA1, PLAG1, SP7, NR2F2, NR2F1, KDM5B, PKNOX1, BRD2, BHLHE40, AR, ZNF324, ZNF366, BRD4, SCRT1, AHR
  • Target gene symbol (double-evidenced CRMs): AP000311.1,SON,ITSN1,AP000295.1,CRYZL1,IFNAR2,DONSON
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 10
  • Number of somatic mutations (non-coding): 1
  • Related genes and loops

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