Deatailed information for cohesin site CDBP00415244


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  • Basic information
  • CohesinDB ID: CDBP00415244
  • Locus: chr21-25506766-25508020
  • Data sourse: ENCSR000BLD, ENCSR000EFJ, GSE93080, ENCSR000EAC, ENCSR000DZP, GSE110061, GSE155324, GSE105028, GSE206145-NatGen2015, ENCSR000ECE, ENCSR000BMY, GSE50893
  • Cell type: GM10847, GM2610, GM19240, H9-hESC, GM2630, Fibroblast, GM2255, IMR-90, GM18486, GM18526, H1-hESC, SNYDER, GM18505, Lymphoblast, GM12878, GM12891, GM2588, GM19239, GM19193, GM19099, GM12892, HCT-116, GM19238, GM18951
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 11% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.733
  • Subunit: SA1,Rad21,SMC1,SA2,Mau2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intergenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: False Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 61% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 87%, "7_Enh": 9%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, PGR, SOX2, XBP1, FOXA1, TSC22D4, NFIC, CHD7, RUNX3, CBFB, PAX5, CDX2, MAF, TEAD1, BCLAF1, TRIM28, SMAD5, USF2, JUN, TCF12, CTCF, SND1, GATA6, IRF4, RAD51, E2F1, PDX1, RBPJ, EED, POU2F2, TOP2A, DUX4, SRF, NBN, ARID3A, ERG2, TBP, HOXC5, ERG, ASCL1, ZNF597, NFKB2, MYC, RAD21, NKX2-1, FOXK2, STAT3, NKX3-1, IKZF1, RCOR1, NR3C1, CEBPB, STAT5B, CREB1, ZHX2, SPI1, EHF, GATA2, DRAP1, RELB, RUNX1, SMC1A, BCL6, CEBPA, NKX2-2, SIN3A, SMAD3, TRIM22, MEF2A, ZBTB2, CREBBP, ZNF384, GATA4, PBX4, DAXX, ATF2, PRDM9, PBX3, FOXM1, ETV6, FOS, CDK8, MED1, PML, SMAD1, NR1H2, SETDB1, STAT5A, ZNF22, MAFK, BCL11A, SP1, NIPBL, REST, ATF7, ASH2L, STAT2, MLLT1, NFATC3, MEF2B, FOXA2, MTA3, EBF1, CREM, NFATC1, E2F8, ZBED1, GTF2B, MEF2C, TCF7, HOXB13, BCL3, YY1, RELA, TARDBP, JUNB, HIF1A, SKIL, GATA3, BATF, MAX, GATA1, PKNOX1, ZNF334, NFKB1, MYOD1, TBX21, BHLHE40, AR, TAF1, ZBTB40, EGR1, IKZF2, JUND, BRD4, CLOCK, ZNF24, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): .
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 10
  • Related genes and loops

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