Deatailed information for cohesin site CDBP00413605


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  • Basic information
  • CohesinDB ID: CDBP00413605
  • Locus: chr21-15848382-15849717
  • Data sourse: GSE138405, GSE206145, GSE206145-NatGen2015, ENCSR000EDE, GSE126990, GSE108869, ENCSR000ECS, GSE165895
  • Cell type: RPE, Hela-Kyoto, Fibroblast, HeLa-S3, HFFc6
  • 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): 0.944
  • Subunit: SA1,Rad21,SMC1,SA2,Mau2,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: 58% Hi-C samples shows Compartment A
  • Cis-regulatory elements
  • Enhancer (Fantom5): non-Enhancer
  • Super enhancer (SEdb): False
  • Chromatin annotation: "5_TxWk": 68%, "7_Enh": 14%,
    Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
  • Co-bound Transcriptional factors: FOXO1, FOSL1, PGR, ZNF660, FOXA1, HNRNPK, ATF3, NFIC, ZNF362, ZBTB44, CHD7, PRDM1, ZNF189, SMARCE1, CDX2, ZNF629, TEAD1, TRIM28, KLF6, SNAI2, ESR1, HNF1B, JUN, TCF12, EP300, BAF155, SOX9, GATA6, DPF2, RFX5, E2F1, PDX1, NANOG, CTBP1, ZNF317, ZBTB48, HIC1, ERG, HOXC5, MYC, ONECUT1, LHX2, RXRA, NKX2-1, STAT3, NKX3-1, RCOR1, ZNF639, VDR, NR3C1, CEBPB, CREB1, GRHL2, ZHX2, IRF1, HDAC2, GATA2, NKX2-2, SIN3A, SMAD3, ZFP37, ZXDC, RUNX2, GATA4, OSR2, SP3, ARNT, PBX4, DAXX, PRDM9, PBX3, SUPT5H, FOS, PIAS1, NR1H2, NUP98-HOXA9, USF1, SP1, RBM22, ZHX1, CTBP2, PHIP, PRDM6, SMC3, ELL2, NCOR2, ZNF394, PPARG, FOXA2, FOXF1, HOXB13, RELA, NEUROD1, JUNB, OTX2, GATA3, TAL1, MAX, TLE3, KLF4, NR2F2, TCF7L2, TP53, PKNOX1, ZNF334, NFKB1, ELF3, BRD2, T, AR, RXR, ZNF366, ZNF280D, BRD4, JUND, CUX1, ZSCAN23, BRCA1, AHR, FOSL2
  • Target gene symbol (double-evidenced CRMs): USP25,NRIP1,HSPA13
  • Function elements
  • Human SNPs: .
  • Number of somatic mutations (coding): 40
  • Number of somatic mutations (non-coding): 0
  • Related genes and loops

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