Deatailed information for cohesin site CDBP00418588


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  • Basic information
  • CohesinDB ID: CDBP00418588
  • Locus: chr21-36757280-36757952
  • Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE72082, ENCSR000BSB, GSE25021, GSE76893, GSE105028, GSE206145, ENCSR000ECE, GSE68388, GSE131606, GSE97394
  • Cell type: MCF-7, H1-hESC, HCT-116, HEK293T, Hep-G2, DKO, HUES64, HuCC-T1, H9-hESC
  • 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): 0.900
  • Subunit: SA1,Rad21,SMC1
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: 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: "5_TxWk": 56%, "15_Quies": 23%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: PGR, SOX2, FOXA1, INSM2, ATF3, ZNF362, CHD7, ZNF189, SMARCE1, ZNF629, TEAD1, TRIM28, KLF6, NFE2L2, ZNF217, ESR1, CTCF, TCF12, JUN, EP300, MNT, SOX4, SMC1, TEAD4, ZNF175, NANOG, CHD8, POU5F1, ZNF317, ZBTB17, ZBTB48, ZSCAN21, SRF, DDX5, SAP130, ERG, MYC, SMARCA4, TSHZ1, RAD21, NKX2-1, GABPA, NKX3-1, RCOR1, ZNF639, NR3C1, CEBPB, CREB1, GRHL2, FEZF1, SPI1, EHF, IRF1, GATA2, FLI1, MRTFB, ZNF554, ETV5, ZNF585A, SMC1A, NKX2-2, SIN3A, ZFX, SMAD3, SMARCC1, ZBTB2, CREBBP, GATA4, OSR2, ZNF184, GR, ARNT, DAXX, PBX4, ATF2, ZEB2, FOS, CDK8, TEAD3, SCRT2, PIAS1, SMAD1, SETDB1, ZNF22, BCL11A, SP1, ATF7, PHIP, SMC3, NCOR2, STAG1, ZNF394, FOXA2, SS18, ZNF600, ZNF30, HOXB13, RELA, HIF1A, OTX2, GATA3, TAL1, MAX, GATA1, SP7, NR2F2, NEUROG2, ZNF334, ELF3, BRD2, BHLHE40, AR, EGLN2, ZNF366, BRD4, JUND, SCRT1, ZNF24, AHR
  • Target gene symbol (double-evidenced CRMs): HLCS
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 6
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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