Deatailed information for cohesin site CDBP00418844


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  • Basic information
  • CohesinDB ID: CDBP00418844
  • Locus: chr21-37396832-37397053
  • Data sourse: ENCSR000BLD, ENCSR000ECE, GSE105028, ENCSR000BKV
  • Cell type: K-562, H1-hESC, H9-hESC
  • 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): 0.967
  • Subunit: Rad21
  • 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: True 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": 41%, "7_Enh": 41%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, PGR, SOX2, XBP1, FOXA1, SUZ12, LEO1, ATF3, ZFP64, ZNF532, MZF1, MITF, TEAD1, TRIM28, ESR1, CTCF, ZNF577, BAF155, NUTM1, E2F1, ZNF528, TFAP2C, POU2F2, CHD8, BRD1, POU5F1, MYCN, TOP2A, ZBTB48, ZSCAN5A, DUX4, ERG, MYC, SMARCA4, HOMEZ, RAD21, GRHL3, NKX2-1, GABPA, STAT3, NKX3-1, HNRNPH1, NR3C1, CEBPB, KMT2A, EZH2, GRHL2, FEZF1, ZNF652, TRPS1, SPI1, HDAC2, GATA2, MXD3, SMARCA5, ZNF490, ZNF766, HEXIM1-CDK9, ETV5, RUNX1, SMC1A, CEBPA, LDB1, ZFX, POU4F2, ZNF534, PCBP2, ZFP37, ERG3, ZNF35, ZNF384, RUNX2, CDK6, GATA4, GR, ARNT, ATF2, PRDM9, HMBOX1, SUPT5H, CDK8, CHD1, TEAD3, TERF1, MYB, SCRT2, PIAS1, RBM22, USF1, BCL11A, REST, ZNF479, PHIP, TCF3, FOXP1, SMC3, STAG1, PPARG, FOXA2, TBL1X, NFATC1, PAF1, ZNF600, WT1, ZBTB33, HOXB13, ZKSCAN1, YY1, RELA, NEUROD1, TCF4, HIF1A, OTX2, TAL1, MAX, GATA1, AGO2, ZNF143, KLF4, SP7, NEUROG2, TP53, ZNF334, MYOD1, PHOX2B, AR, ZBTB26, NOTCH3, BRD4, SCRT1, MAZ, AHR
  • Target gene symbol (double-evidenced CRMs): VPS26C,TTC3,DYRK1A
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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