Deatailed information for cohesin site CDBP00413718


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  • Basic information
  • CohesinDB ID: CDBP00413718
  • Locus: chr21-16305493-16308786
  • Data sourse: ENCSR000BTU, ENCSR230ZWH, GSE131956, GSE138405, GSE126634, ENCSR404BPV, GSE152721, GSE62063, ENCSR198ZYJ, GSE126990, ENCSR917QNE
  • Cell type: Hela-Kyoto, Neurons-H1, Ishikawa, GBM39, Liver, HAP1, Ramos
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 3% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.922
  • Subunit: NIPBL,SMC3,Rad21,SA2
  • 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: True ChIA-PET loops: True
  • Compartment: 40% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 37%, "1_TssA": 25%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: PGR, CBX5, ZNF660, SOX2, FOXA1, ATF3, NFIC, CHD7, PRDM1, ZBTB44, RUNX3, SMARCE1, PAX5, TP63, MITF, SFPQ, ELF1, ETV1, ESR1, OCA2, TP73, JUN, CTCF, TCF12, BAF155, EP300, IRF4, RFX5, E2F1, TEAD4, RBPJ, TFAP2C, NANOG, CHD8, BRD3, TOP2A, ZBTB17, DUX4, STAT1, SRF, HNF4G, ERG, ONECUT1, MYC, SMARCA4, RAD21, LHX2, RXRA, NKX2-1, BATF3, GABPA, STAT3, NKX3-1, VDR, NR3C1, CEBPB, CREB1, EZH2, GATA2, FLI1, ZNF777, MXI1, MRTFB, MYF5, EZH2phosphoT487, ZFX, POU4F2, SMAD3, SMARCC1, RUNX2, ARNT, ATF2, FOXM1, CHD1, CDK8, FOS, MED1, CSNK2A1, PML, PIAS1, KLF9, L3MBTL2, NUP98-HOXA9, MAFK, SP1, NIPBL, USF1, HNF4A, REST, ARID1A, ATF7, POU2F3, ASH2L, HOXA9, BCOR, FOXP1, PRDM6, FOXA2, MTA3, CREM, SS18, GTF2B, ZBTB33, CDK9, HOXB13, YY1, RELA, NEUROD1, JUNB, BRG1, HIF1A, OTX2, BATF, TAL1, MAX, ZSCAN26, TLE3, KLF4, SP7, NR2F2, PKNOX1, PHOX2B, T, BRD2, AR, EGLN2, NOTCH3, BRD4, JUND, BRCA1, FOSL2
  • Target gene symbol (double-evidenced CRMs): .
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 5
  • Related genes and loops

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