Deatailed information for cohesin site CDBP00413778


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  • Basic information
  • CohesinDB ID: CDBP00413778
  • Locus: chr21-16536082-16538207
  • Data sourse: GSE131956, GSE138405, GSE126634, ENCSR000BLY, GSE206145, GSE62063, ENCSR000EDE, ENCSR000EHX, GSE138105, GSE126990, GSE108869, ENCSR000ECS, ENCSR917QNE
  • Cell type: RPE, Hela-Kyoto, SLK, HeLa-S3, GBM39, SK-N-SH, Liver, HAP1, Ramos
  • 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,SA2,Mau2,SMC3
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: TSS,TES
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 40% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 41%, "1_TssA": 31%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, FOSL1, PGR, ZNF660, SOX2, XBP1, PATZ1, FOXA1, ZFHX2, ATF3, NFIC, ZNF362, ZBTB44, PRDM1, RUNX3, MORC2, ZNF189, ZSCAN4, MITF, SFPQ, ZNF629, TEAD1, KLF6, NFE2L2, ESR1, OCA2, MED26, PITX3, USF2, JUN, CTCF, TCF12, EP300, BAF155, RFX5, E2F1, TEAD4, GTF2F1, RBPJ, EED, POU2F2, CHD8, BRD3, ZNF263, TOP2A, MYCN, ZSCAN21, ZBTB17, ZBTB48, DUX4, STAT1, SRF, HIC1, TBP, ERG, ZBTB21, HOXC5, ETS1, MYC, ONECUT1, SMARCA4, ZKSCAN2, RFX1, RAD21, TOP1, GRHL3, RXRA, NKX2-1, STAT3, UBN1, NKX3-1, NFE2, RCOR1, ZNF639, ARNTL, NR3C1, CEBPB, ZNF750, CREB1, EZH2, KLF8, GRHL2, EBF3, ZHX2, SPI1, GATA2, ZNF182, FLI1, MXI1, MRTFB, MYF5, RUNX1, SMC1A, CEBPA, NKX2-2, SIN3A, AFF4, POU4F2, ZNF335, ZFP37, ERG3, TWIST1, SMARCC1, PRDM10, ZNF384, ZNF35, RUNX2, ZNF184, NRF1, BACH1, ARNT, NFIB, PBX4, ATF2, ZNF518A, FOXM1, PBX3, SP2, CHD1, CDK8, FOS, MED1, CSNK2A1, ZEB1, CEBPD, ZXDB, PIAS1, KLF9, NUP98-HOXA9, MAFK, SP1, USF1, BCL11A, HNF4A, REST, ZNF479, ZHX1, POU2F3, ASH2L, CTBP2, PHIP, FOXP1, PRDM6, SMC3, ELL2, ZNF394, PPARG, FOXA2, EBF1, CHD2, SS18, ZNF600, ZNF692, MAFF, WT1, ZBTB33, HOXB13, KDM1A, YY1, RELA, NEUROD1, JUNB, BRG1, ISL1, HIF1A, OTX2, GATA3, TAL1, MAX, GATA1, HAND2, TLE3, KLF4, SP7, NCOA3, NR2F2, NEUROG2, TP53, ZBTB6, NFKB1, MYOD1, ZSCAN22, PHOX2B, BRD2, ARRB1, AR, PAX3-FOXO1, TAF1, ZNF324, EGLN2, ZNF366, ZNF280D, MYNN, NOTCH3, BRD4, JUND, MAZ, ZSCAN23, BRCA1, ZNF316
  • Target gene symbol (double-evidenced CRMs): .
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 16
  • Related genes and loops

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