Deatailed information for cohesin site CDBP00416175


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00416175
  • Locus: chr21-29268171-29268856
  • Data sourse: ENCSR000BLD, ENCSR230ZWH, GSE72082, ENCSR000EGW, ENCSR000BLY, GSE105028, GSE121355, GSE25021, GSE108869, ENCSR917QNE, GSE93080, ENCSR000DZP, ENCSR000EAC, GSE143937, ENCSR000BKV, GSE86191, GSE138405, GSE76893, GSE101921, GSE206145-NatGen2015, GSE94872, ENCSR000EEG, GSE98367, ENCSR879KXD, ENCSR000BLS, ENCSR000EHW, GSE206145, ENCSR000EHX, ENCSR217ELF, ENCSR000BTQ, ENCSR167MTG, GSE129526, ENCSR054FKH, ENCSR000EDE, GSE68388, GSE126990, GSE50893
  • Cell type: GM10847, GM2610, GM19240, Liver, HuCC-T1, H9-hESC, RPE, GM2630, Fibroblast, HeLa-S3, GM2255, K-562, GM18486, H1-hESC, SNYDER, GM12878, GM2588, SK-N-SH, GM19239, GM19193, Macrophage, MCF-7, GM12892, Hela-Kyoto, HCT-116, Hep-G2, A-549, HUVEC, HCAEC
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 15% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.678
  • Subunit: SA1,Rad21,SMC1,SA2,SMC3
  • CTCF binding site: CTCF CTCF motif: False
  • Genomic location: Intragenic
  • 3D genome
  • TAD boundary: non-Boundary
  • Chromatin hubs: non-Hub
  • Hi-C loops: False Hi-ChIP loops: False ChIA-PET loops: True
  • Compartment: 68% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "15_Quies": 93%, "7_Enh": 5%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: ZNF283, PGR, POU2F2, SMC1A, FOXA2, XBP1, DUX4, FOXF1, FOXA1, HOXB13, ERG, RELA, ZBTB2, ASCL1, MYC, RUNX2, GATA4, RFX1, RAD21, GRHL3, OTX2, GATA3, TAL1, TP63, GATA1, ZNF143, RCOR1, NFE2, SFPQ, TLE3, TEAD1, ZNF680, SNAI2, SMAD1, CTCF, BAF155, BCL11A, KLF1, AR, GATA2, REST, EGLN2, BRD4, PHIP, SMC1, SMC3, STAG1
  • Target gene symbol (double-evidenced CRMs): BACH1
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 0
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

eachgene