Deatailed information for cohesin site CDBP00420271


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  • Basic information
  • CohesinDB ID: CDBP00420271
  • Locus: chr21-42208748-42210810
  • Data sourse: ENCSR895JMI, ENCSR853VWZ, GSE206145-GSE177045, GSE67783, GSE86191, ENCSR944ZCT, ENCSR501LQA, GSE98367, ENCSR768DOX, GSE101921, ENCSR981FDC, ENCSR247LSH, ENCSR000EDE, ENCSR153HNT, ENCSR620NWG, ENCSR748MVX, ENCSR000ECS
  • Cell type: MCF-7, HCT-116, A-549, HCAEC, HeLa-S3, K-562, HSPC, Macrophage
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 7% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.911
  • Subunit: SA1,Rad21,SMC1,Mau2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 94% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 46%, "14_ReprPCWk": 27%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: PGR, SOX2, XBP1, FOXA1, CHD7, TEAD1, ETV1, NFE2L2, ESR1, CTCF, JUN, TCF12, EP300, SMC1, TEAD4, TFAP2C, GLIS1, POU2F2, CHD8, ZNF263, MYCN, POU5F1, TOP2A, ZBTB48, DUX4, HOXC5, ERG, ETS1, MYC, SMARCA4, GRHL3, NKX2-1, GABPA, STAT3, XRCC5, PRDM14, IKZF1, HNRNPH1, NR3C1, ESRRA, CEBPB, CREB1, GRHL2, SPI1, GATA2, NR2C2, NCOA2, RUNX1, SMC1A, CBX1, AFF4, ZFX, SIN3A, SMAD3, ERG3, ZNF18, SMARCC1, CREBBP, PBX4, ARNT, HMGB2, ETV6, FOS, MED1, TFAP2A, HNF4A, REST, ARID1A, ZHX1, CTBP2, SMC3, STAG1, TBL1X, FOXA2, WT1, FOXF1, YY1, RELA, SP140, HIF1A, GATA3, TAL1, NRIP1, NCOA3, NR2F2, NR2F1, TCF7L2, ZNF334, ELF3, ARRB1, AR, HSF1, ZBTB26, BRD4, MAZ, AHR
  • Target gene symbol (double-evidenced CRMs): MX1,ABCG1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 14
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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