Deatailed information for cohesin site CDBP00418617


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  • Basic information
  • CohesinDB ID: CDBP00418617
  • Locus: chr21-36823587-36823665
  • Data sourse: GSE120943, GSE98367
  • Cell type: Monocytes, Macrophage
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 1% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.978
  • Subunit: SMC1
  • CTCF binding site: non-CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: False 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": 63%, "5_TxWk": 35%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: NFIA, PATZ1, FOXA1, LEO1, ZFHX2, ATF3, NFIC, CHD7, CBFB, ZSCAN4, HDAC3, ZNF26, SAP30, ESR1, MLL, TP73, USF2, CTCF, TCF12, EP300, BAF155, ZBTB20, MNT, RYBP, E2F6, ZNF423, ZNF350, TEAD4, PDX1, JARID2, GLIS1, CHD8, BRD1, ZSCAN5D, ZNF263, MYCN, POU5F1, TOP2A, ZBTB17, ZBTB48, ZSCAN5A, STAT1, DUX4, ERG2, SP4, ERG, ASCL1, OGG1, ZBTB8A, MYC, ONECUT1, SMARCA4, RAD21, GRHL3, APC, STAT3, NKX3-1, ZNF398, VDR, CEBPB, CREB1, FEZF1, GABPB1, SPI1, HDAC2, GATA2, FLI1, MXI1, MRTFB, ZNF554, RUNX1, SMC1A, NKX2-2, SIN3A, ZFX, TET2, ERG3, PRDM10, RARA, RUNX2, CDK6, GATA4, OSR2, NCAPH2, CDK8, ZXDB, MYB, SCRT2, ZMYM3, PIAS1, KLF9, ZNF41, EVI1, RBM22, SP1, BCL11A, RBM25, PHIP, BCOR, GLIS2, FOXP1, AATF, SMC3, STAG1, TRP47, CBFA2T2, TBL1X, FOXA2, RBBP5, PAF1, ZNF600, ZNF692, WT1, HOXB13, KDM1A, YY1, RELA, SP140, ZFP36, ZIC2, HIF1A, OTX2, ZNF519, TAL1, MAX, ZNF143, AGO2, PLAG1, MYOD1, EGR2, BRD2, AR, RXR, ZBTB42, HEXIM1, ZNF366, TFIIIC, HSF1, NOTCH3, BRD4, MAZ, 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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