Deatailed information for cohesin site CDBP00417031


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00417031
  • Locus: chr21-32592176-32593983
  • Data sourse: ENCSR167MTG, ENCSR000EEG, ENCSR338DUC, ENCSR230ZWH, GSE67783, GSE72082, GSE165895, GSE86191, GSE111913, GSE76893, ENCSR000BLS, GSE206145, ENCSR054FKH, ENCSR153HNT, GSE112028, GSE25021, ENCSR000EDW, ENCSR917QNE
  • Cell type: RPE, HCT-116, Hep-G2, RT-112, Liver, K-562, HeLa-Tet-On, HSPC, HFFc6
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 6% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.900
  • Subunit: NIPBL,SA1,Rad21,SMC1,SA2,SMC3
  • 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: 90% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 41%, "5_TxWk": 34%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: NFIA, PGR, HMG20A, HNF1A, ZNF101, FOXA1, SUZ12, RBFOX2, RXRB, KDM3A, TFAP4, HDGF, TSC22D4, ATF3, NFIC, THRB, PRDM1, ATF4, CDX2, TEAD1, ELF1, TRIM28, RBM39, KLF6, SNAI2, RCOR2, ESR1, OCA2, MED26, CTCF, TCF12, EP300, SOX5, GATA6, E2F6, DMAP1, FOXA3, ZNF175, GATAD2A, EHMT2, RBPJ, GTF2F1, PDX1, MLX, MYCN, HHEX, RUNX1T1, TOP2A, ZNF263, MTA2, ZBTB48, ZSCAN5A, GATAD1, DDX5, NBN, SAP130, ARID3A, TBP, HNF4G, ETS1, MYC, SMARCA4, RAD21, GRHL3, RXRA, NKX2-1, GABPA, STAT3, ZNF614, XRCC5, IKZF1, MIER3, HNRNPH1, NR2F6, RCOR1, VDR, NR3C1, CEBPB, CREB1, CCAR2, TBL1XR1, ZNF652, GABPB1, ZHX2, MIXL1, TFE3, HDAC2, GATA2, ZNF644, MXD3, DRAP1, ZGPAT, NFIL3, ETV5, THAP11, BCL6, SMC1A, HDAC1, CEBPA, SOX13, ZFX, ERG3, SP5, SMARCC1, MYBL2, RARA, ZNF384, CDK6, GATA4, ARNT, ZNF48, SMAD4, FOS, HMGXB4, SMARCB1, MED1, TEAD3, ZEB1, SCRT2, ZMYM3, U2AF1, SMAD1, ZNF41, RBM22, BCL11A, SP1, NIPBL, HNF4A, ARID2, IKZF5, REST, ZBTB7A, ASH2L, FOXP1, SMC3, STAG1, ETV4, SKI, TRP47, PPARG, FOXA2, CREM, MIER2, WT1, FOXF1, ZBTB33, TCF7, HOXB13, ZKSCAN1, FOXO3, KDM1A, YY1, ZNF580, ZNF19, RELA, SP140, HIF1A, MAX, GATA1, MTA1, CBX2, CEBPG, NR2F2, ZNF512, NR2F1, NEUROG2, ZNF334, MYOD1, ELF3, PHF5A, KAT8, ARID4B, BHLHE40, NFKBIZ, AR, ZNF366, EGR1, ZBTB26, BRD4, JUND, SCRT1, CUX1, MAZ, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): URB1,MIS18A,TIAM1,EVA1C,SCAF4,CFAP298-TCP10L,HUNK
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 20
  • Number of somatic mutations (non-coding): 6
  • Related genes and loops

eachgene