Deatailed information for cohesin site CDBP00416782


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  • Basic information
  • CohesinDB ID: CDBP00416782
  • Locus: chr21-31932637-31934436
  • Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE104888, ENCSR230ZWH, GSE72082, ENCSR000BSB, GSE116868, ENCSR000EGW, ENCSR000BLY, GSE105028, GSE121355, GSE103477, GSE111537, GSE131606, GSE108869, ENCSR000EDW, GSE25021, ENCSR000BUC, ENCSR917QNE, ENCSR000EFJ, ENCSR000BTU, GSE93080, GSE143937, GSE67783, ENCSR000BKV, GSE115250, GSE138405, GSE86191, GSE76893, GSE101921, GSE152721, GSE206145-NatGen2015, GSE130135, ENCSR703TNG, GSE106870, GSE116344, GSE145327, GSE94872, ENCSR000EEG, ENCSR338DUC, ENCSR193NSH, ENCSR768DOX, ENCSR879KXD, ENCSR000BLS, ENCSR000EHW, GSE206145, ENCSR000ECE, ENCSR247LSH, ENCSR000BMY, ENCSR000EHX, GSE97394, ENCSR217ELF, ENCSR000BTQ, GSE55407, ENCSR167MTG, ENCSR956LGB, GSE110061, GSE129526, ENCSR000HPG, ENCSR335RKQ, ENCSR054FKH, ENCSR000EDE, ENCSR153HNT, GSE68388, GSE83726, GSE126990, GSE50893, GSE131577
  • Cell type: MDM, RH4, GM2610, CVB-hiPSC, GM19240, HSPC, Liver, TC-32, HuCC-T1, H9-hESC, GM2630, Fibroblast, Ishikawa, HeLa-S3, IMR-90, K-562, DKO, H1-hESC, MB157, GM12878, SK-N-SH, THP-1, HUES64, MCF-7, GM12892, Hela-Kyoto, HCT-116, HL-60, HEK293T, Hep-G2, A-549, HUVEC, HCAEC, OCI-AML-3, HAP1
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 29% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.600
  • Subunit: SA1,Rad21,SMC1,SA2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: non-Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 71% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 44%, "5_TxWk": 23%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: SMC1A, FOXA2, ZNF263, CREM, POU5F1, TEAD4, CTBP1, SMAD3, FOXA1, FOXF1, SRF, ERG3, SUZ12, ZNF134, PBX2, ARID3A, HOXB13, ERG2, PRDM10, ERG, KDM1A, HOXC5, ZBTB2, ZNF384, ZNF35, YY1, ZNF341, NEUROD1, MYC, RAD21, SP140, ARNT, HIF1A, OTX2, NKX2-1, GATA3, XRCC5, ZNF614, NKX3-1, ZNF143, HMGXB4, RCOR1, GATA1, MITF, ZNF467, GFI1B, TEAD3, TCF7L2, NFE2L2, CCAR2, EZH2, ESR1, OCA2, KLF9, CTCF, ELF3, BRD2, SP1, BAF155, SPI1, BHLHE40, BCL11A, REST, GATA2, SOX6, ASH2L, NCOR1, JUND, MAZ, SMC1, SMC3, STAG1, AHR
  • Target gene symbol (double-evidenced CRMs): HUNK
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 10
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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