Deatailed information for cohesin site CDBP00418621


Check detailed explainations here

  • Basic information
  • CohesinDB ID: CDBP00418621
  • Locus: chr21-36835469-36835862
  • Data sourse: GSE86191, ENCSR000EDE, GSE83726, GSE130135, GSE116344, GSE25021, ENCSR000ECS
  • Cell type: MCF-7, RH4, HCT-116, HEK293T, HeLa-S3
  • DNA Sequence of binding site: UCSC hg38
  • Cohesin category
  • Peak occupancy ratio: 2% samples have this site.
  • Cell specificity (0: conserved, 1: cell type specific): 0.944
  • Subunit: SMC3,Rad21,SA1
  • CTCF binding site: CTCF CTCF motif: False
  • 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: 94% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): True
  • Chromatin annotation: "15_Quies": 65%, "5_TxWk": 20%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, PGR, ZNF660, XBP1, PATZ1, FOXA1, MLL4, TFAP4, ZFP64, ZBTB44, IKZF3, ZNF273, ZNF189, ZNF320, ZNF467, CDX2, ZNF629, KLF5, ZNF121, KLF10, ZNF561, CTCF, TCF12, BAF155, KLF1, ZBTB20, E2F1, ZNF528, TFAP2C, GLIS1, NANOG, CHD8, ZNF263, ZSCAN21, ZBTB17, ZBTB48, ZSCAN5A, ZNF317, SP4, ERG, ZBTB21, ZNF585B, ZBTB8A, ZNF341, MYC, RAD21, GRHL3, GABPA, NKX3-1, ZNF750, ZNF93, CREB1, EZH2, FEZF1, KLF17, GATA2, ZNF582, ZNF554, SIN3A, ZFX, AFF4, PRDM10, CREBBP, ZNF35, NOTCH1, RUNX2, CDK6, OSR2, ZNF184, SP3, PBX4, ARNT, ZEB2, SP2, CDK8, CEBPD, MYB, SCRT2, PIAS1, KLF9, BCL11A, ZNF479, ASH2L, PHIP, PRDM6, SMC3, STAG1, ZNF394, ZNF600, ZSCAN16, ZNF692, WT1, HOXB13, YY1, RELA, SP140, TCF4, ZIC2, HIF1A, GATA3, KLF15, MAX, ZNF143, HAND2, KLF4, SP7, NCOA3, NEUROG2, KDM5B, TP53, PKNOX1, ZBTB6, MYOD1, ZNF843, AR, ZNF324, EGLN2, ZBTB42, ZBTB26, NCOR1, SCRT1, BRD4, MAZ, ZNF24
  • Target gene symbol (double-evidenced CRMs): HLCS
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 3
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

eachgene