Deatailed information for cohesin site CDBP00419393


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  • Basic information
  • CohesinDB ID: CDBP00419393
  • Locus: chr21-39091863-39092124
  • Data sourse: GSE206145-NatGen2015, GSE67783, GSE38411
  • Cell type: BCBL-1, Fibroblast, 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): 0.967
  • Subunit: SA1,SA2,SMC1
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intergenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 96% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 57%, "5_TxWk": 24%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, NFIA, PGR, HMG20A, SUZ12, RXRB, UBTF, KDM3A, ATF3, NFIC, ZFP64, THAP1, MXD4, ZNF189, ZNF506, TEAD1, TRIM28, RBM39, SNAI2, NFE2L2, RCOR2, ESR1, JUN, CTCF, EP300, SOX5, PAX8, E2F1, SMC1, FOXA3, GATAD2A, RBPJ, TFAP2C, ZSCAN5D, MYCN, ZNF263, CTBP1, ZBTB48, STAT1, GATAD1, SAP130, ERG, MYC, HOMEZ, RAD21, STAT3, XRCC5, UBN1, ZNF614, IKZF1, MIER3, RCOR1, ZNF639, NR2F6, NR3C1, CEBPB, CREB1, CCAR2, ZNF652, GABPB1, ZHX2, SPI1, MIXL1, EHF, GATA2, ZNF644, MXD3, DRAP1, ZGPAT, NFIL3, ZNF554, ETV5, BCL6, SMC1A, CEBPA, CBX1, SOX13, ZFX, ZNF770, CBX8, SP5, RARA, NFYC, ZBTB2, RUNX2, ZNF184, PBX4, DAXX, TFDP1, ZNF48, SMAD4, FOS, CDK8, HMGXB4, TEAD3, ZMYM3, ZNF3, L3MBTL2, MAFK, NIPBL, HNF4A, IKZF5, REST, ZNF548, SMC3, STAG2, STAG1, MLLT1, NFATC3, SKI, PPARG, FOXA2, MTA3, MIER2, WT1, MEF2C, ZNF580, KDM1A, RELA, JUNB, NEUROD1, MCM3, SP140, ZFP36, HIF1A, SKIL, GATA3, TAL1, MAX, NRIP1, ZNF143, GATA1, CEBPG, NR2F1, KDM5B, TP53, ELF3, ARID4B, AR, BHLHE40, NFKBIZ, RB1, ZBTB26, HSF1, NCOR1, JUND, BRD4, MAZ, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): ETS2
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 4
  • Related genes and loops

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