Deatailed information for cohesin site CDBP00416629


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  • Basic information
  • CohesinDB ID: CDBP00416629
  • Locus: chr21-31524208-31524413
  • Data sourse: ENCSR000BLD, ENCSR000ECE
  • Cell type: H1-hESC
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 0% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.989
  • Subunit: Rad21
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 67% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 70%, "7_Enh": 12%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOSL1, PGR, MEIS2, XBP1, PATZ1, FOXA1, ZFHX2, ATF3, ZNF362, ZBTB44, PRDM1, CHD7, ZNF189, MITF, ZNF629, KLF5, TEAD1, TRIM28, NFE2L2, ESR1, ZNF561, CTCF, JUN, EP300, KLF1, RYBP, SOX4, E2F6, ZNF423, E2F1, ZNF528, TFAP2C, GLIS1, NANOG, CHD8, POU2F2, ZSCAN5D, POU5F1, TOP2A, CTBP1, ZNF317, ZBTB17, ZBTB48, SRF, DDX5, ERG2, SP4, HIC1, ERG, ZNF341, MYC, EOMES, KDM4A, RAD21, GRHL3, RXRA, STAT3, CREB1, EZH2, KLF8, GRHL2, HDAC2, GATA2, FLI1, ZNF490, MRTFB, NCOA2, ZNF554, CBX1, SMC1A, ZFX, SMAD3, ERG3, PRDM10, CREBBP, ZNF384, ZNF35, OSR2, ZNF184, SP3, ZBTB10, ZEB2, FOXM1, SP2, FOS, CDK8, MED1, ICE2, ZNF264, ZNF680, SCRT2, KLF9, SETDB1, KLF16, SP1, NIPBL, TFAP2A, HNF4A, REST, CTBP2, PHIP, GLIS2, FOXP1, MBD2, STAG1, FOXA2, CBX3, CHD2, PAF1, ZNF600, ZNF692, WT1, CDK9, HOXB13, YY1, RELA, AHR, ZIC2, HIF1A, OTX2, GATA3, KLF15, TAL1, MAX, NRIP1, TLE3, SP7, NCOA3, NR2F2, NR2F1, TCF7L2, KDM5B, TP53, ZNF334, EGR2, BRD2, T, AR, ZNF324, ZBTB42, EGR1, HEXIM1, MYNN, HSF1, NOTCH3, JUND, BRD4, SCRT1, MAZ, ZNF316, FOSL2
  • Target gene symbol (double-evidenced CRMs): TIAM1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 2
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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