Deatailed information for cohesin site CDBP00419726


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  • Basic information
  • CohesinDB ID: CDBP00419726
  • Locus: chr21-40318353-40327457
  • Data sourse: ENCSR000BLD, ENCSR000BTQ, GSE206145-GSE177045, GSE67783, GSE72082, GSE86191, GSE76893, GSE105028, ENCSR000ECE, ENCSR703TNG, GSE25021, GSE115602
  • Cell type: MCF-7, H1-hESC, HCT-116, HSPC, H9-hESC
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 9% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.944
  • Subunit: NIPBL,SA1,Rad21,SMC1,Mau2
  • CTCF binding site: CTCF CTCF motif: True
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 33% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 68%, "9_Het": 24%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: MBD3, PGR, ZNF496, FOXA1, MEN1, WDHD1, DPF1, SMARCE1, TEAD1, ZNF217, ESR1, CTCF, TCF12, JUN, EP300, BAF155, MNT, DPF2, MED12, RAD51, PRKDC, ZNF512B, NR5A2, TEAD4, TFAP2C, CHD8, CTBP1, DUX4, UTX, SRF, ERG, RAD21, GABPA, NKX3-1, RCOR1, ZNF750, ESRRA, CEBPB, NR3C1, CREB1, GRHL2, TRPS1, ZHX2, ZSCAN2, KDM5A, HDAC2, GATA2, GATAD2B, SREBF1, SMARCA5, NCOA2, RUNX1, SMC1A, CBX1, SIN3A, NFXL1, ZXDC, ZNF384, CREBBP, GR, ARNT, NFIB, PRDM9, FOXM1, ETV6, CHD1, FOS, MED1, PML, ZMYM3, PIAS1, NCOA1, NIPBL, TFAP2A, REST, ARID1A, ATF7, CTBP2, MBD2, FOXP1, STAG1, MLLT1, ZNF283, FOXA2, MTA3, HOXB13, RELA, TARDBP, NEUROD1, HIF1A, GATA3, MAX, NRIP1, MTA1, TLE3, ZNF592, NCOA3, NR2F2, TCF7L2, NR2F1, ZNF687, TP53, AR, ZBTB40, YAP1, EGLN2, HSF1, BRD4, JUND, CLOCK, CUX1, ZNF24, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): .
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 168
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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