Deatailed information for cohesin site CDBP00416797


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00416797
  • Locus: chr21-31985307-31986138
  • Data sourse: ENCSR000BLD, GSE67783, ENCSR000BKV, GSE86191, GSE105028, GSE206145, GSE116344, GSE38411
  • Cell type: RPE, H1-hESC, HCT-116, RH4, K-562, BCBL-1, HSPC, 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): 0.911
  • Subunit: SA1,Rad21,SMC1
  • CTCF binding site: CTCF CTCF motif: True
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: Hub
  • Hi-C loops: True Hi-ChIP loops: True ChIA-PET loops: True
  • Compartment: 71% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 53%, "5_TxWk": 20%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: PGR, XBP1, PATZ1, FOXA1, ATF3, CTCFL, PRDM1, CBFB, ZNF467, KLF5, TEAD1, KLF6, RBM39, ESR1, OCA2, CTCF, JUN, KLF1, MNT, ZNF512B, TFAP2C, POU2F2, CHD8, ZSCAN5D, MYCN, ZNF263, TOP2A, RUNX1T1, POU5F1, ZBTB17, ZBTB48, ZSCAN5A, STAT1, DDX5, ERG, MYC, ONECUT1, SMARCA4, RAD21, GRHL3, XRCC5, NKX3-1, HNRNPH1, ZNF639, NR3C1, ESRRA, EZH2, KLF8, GRHL2, TRPS1, HDAC2, GATA2, FLI1, NCOA2, RUNX1, SMC1A, EZH2phosphoT487, CRY1, SIN3A, ZFX, TET2, ERG3, ZNF770, SMARCC1, CREBBP, GR, ARNT, FOS, SCRT2, RBM22, TFAP2A, REST, CTBP2, AATF, SMC3, STAG1, TRP47, FOXA2, ZNF600, WT1, HOXB13, YY1, RELA, MCM3, SP140, HIF1A, GATA3, TAL1, MAX, NRIP1, ZNF143, AGO2, TLE3, KLF4, NCOA3, NR2F2, ZNF512, NR2F1, ARRB1, AR, PAX3-FOXO1, ZNF366, HSF1, NOTCH3, BRD4, SCRT1, CLOCK, MAZ, AHR
  • Target gene symbol (double-evidenced CRMs): CFAP298,MIS18A,CFAP298-TCP10L,SYNJ1,HUNK
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 13
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

eachgene