Deatailed information for cohesin site CDBP00413395


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  • Basic information
  • CohesinDB ID: CDBP00413395
  • Locus: chr21-15014507-15017598
  • Data sourse: ENCSR000EFJ, ENCSR956LGB, GSE206145-GSE177045, ENCSR501LQA, ENCSR000HPG, ENCSR676MJK, GSE206145, GSE85526, ENCSR981FDC, GSE206145-NatGen2015, ENCSR198ZYJ, GSE68388, GSE165895
  • Cell type: MCF-7, RPE, Fibroblast, HEKn, Neurons-H1, A-549, IMR-90, HuCC-T1, HFFc6
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 6% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.900
  • Subunit: NIPBL,SA1,Rad21,SMC1,SA2,Mau2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: TSS
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 52% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "5_TxWk": 50%, "15_Quies": 26%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, PGR, SOX2, FOXA1, MEN1, ATF3, CHD7, PRDM1, TP63, TEAD1, KLF6, SNAI2, ESR1, HNF1B, CTCF, JUN, TCF12, EP300, TEAD4, GATAD2A, PDX1, POU2F2, TOP2A, DUX4, SRF, ERG, HOXC5, ETS1, MYC, SMARCA4, RAD21, LHX2, GRHL3, NKX2-1, GABPA, STAT3, RCOR1, VDR, NR3C1, CEBPB, ZNF750, KMT2A, MRTFA, ZHX2, SPI1, IRF1, GATA2, SIX2, FLI1, ZNF766, MRTFB, BCL6, MAFG, CEBPA, SMC1A, EZH2phosphoT487, SIN3A, SMAD3, ZNF770, ZNF792, RUNX2, GATA4, ARNT, PBX4, FOS, CDK8, MED1, CEBPD, SUPT16H, C11orf30, RBM22, MAFK, HNF4A, MLLT1, PAX7, FOXA2, PAF1, GTF2B, MAFF, KDM1A, RELA, NEUROD1, JUNB, HIF1A, OTX2, GATA3, MAX, AGO2, HAND2, CEBPG, KLF4, TP53, NFKB1, MYOD1, PHOX2B, BRD2, BHLHE40, AR, BRD4, ZNF316, FOSL2
  • Target gene symbol (double-evidenced CRMs): NRIP1
  • Function elements
  • Human SNPs: Heart_rate_response_to_beta_blockers_(atenolol_monotherapy)
  • Number of somatic mutations (coding): 63
  • Number of somatic mutations (non-coding): 21
  • Related genes and loops

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