Deatailed information for cohesin site CDBP00420175


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  • Basic information
  • CohesinDB ID: CDBP00420175
  • Locus: chr21-41883793-41886940
  • Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE72082, GSE116868, GSE105028, GSE121355, GSE25021, GSE131606, ENCSR000EDW, GSE93080, GSE67783, GSE86191, GSE76893, GSE206145-NatGen2015, ENCSR703TNG, GSE98367, ENCSR000BLS, GSE206145, ENCSR000ECE, ENCSR000BMY, GSE97394, ENCSR000BTQ, ENCSR167MTG, GSE129526, ENCSR153HNT, GSE83726, GSE50893
  • Cell type: RH4, GM10847, GM2610, GM19240, HSPC, H9-hESC, RPE, Fibroblast, GM12890, GM2255, K-562, GM18486, DKO, GM18526, H1-hESC, SNYDER, MB157, GM12878, GM12891, GM2588, GM19239, GM19193, GM19099, HUES64, Macrophage, GM12892, MCF-7, HCT-116, Hep-G2, GM19238, GM18951
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 14% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.656
  • Subunit: SA1,Rad21,SMC1,SA2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: TSS,TES
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 96% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "5_TxWk": 53%, "15_Quies": 21%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, FOSL1, ZSCAN5C, XBP1, FOXA1, ATF3, RUNX3, TP63, JMJD1C, RBM39, SNAI2, ESR1, OCA2, CTCF, JUN, TCF12, LMO1, IRF4, FOXA3, GATAD2A, POU2F2, CHD8, BRD1, MYCN, POU5F1, ZBTB48, ZSCAN5A, ERG, PBX1, ASCL1, OGG1, MYC, SMARCA4, RAD21, GRHL3, GABPA, STAT3, XRCC5, IKZF1, HNRNPH1, NR3C1, CEBPB, KMT2A, CREB1, BMPR1A, ZNF652, GABPB1, SPI1, GATA2, MXD3, SIX2, FLI1, NCOA2, RUNX1, SMC1A, CEBPA, FIP1L1, ZFX, SOX13, TET2, ZNF549, ZBTB2, NOTCH1, ARNT, ZNF48, FOS, CDK8, MED1, TEAD3, KDM6B, MYB, SCRT2, NCOA1, RBM22, BCL11A, IKZF5, PHIP, TCF3, FOXP1, AATF, SMC3, STAG1, NFATC3, TRP47, FOXA2, TBL1X, PAF1, ZNF600, WT1, FOXF1, CDK9, YY1, RELA, NEUROD1, SP140, TCF4, OTX2, TAL1, AGO2, HAND2, BCL11B, ZNF334, BHLHE40, PAX3-FOXO1, ZBTB40, RXR, HSF1, ZBTB26, BRD4, SCRT1, MAZ, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): C2CD2,ZBTB21,UMODL1,PRDM15
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 32
  • Number of somatic mutations (non-coding): 19
  • Related genes and loops

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