- Basic information
- CohesinDB ID: CDBP00420723
- Locus: chr21-43578473-43579527
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Data sourse: ENCSR000BTQ, GSE206145-GSE177045, GSE72082, GSE86191, GSE76893, GSE206145, GSE206145-NatGen2015, ENCSR703TNG
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Cell type: MCF-7, Fibroblast, HCT-116, RPE
- DNA Sequence of binding site:
UCSC hg38
- Cohesin category
- Peak occupancy ratio: 4% samples have this site.
- Cell specificity (0: conserved, 1: cell type specific): 0.956
- Subunit: NIPBL,SA1,Rad21,SA2,Mau2
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intragenic
- 3D genome
- TAD boundary: non-Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
70% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): True
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Chromatin annotation:
"15_Quies": 60%,
"5_TxWk": 15%,
Note: The percentage represent how many of the 127 Roadmap datasets show the indicated state (top 2).
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Co-bound Transcriptional factors: MBD3, FOXO1, FOSL1, PGR, ZSCAN5C, SOX2, XBP1, FOXA1, HLF, SUZ12, ZFHX2, TFAP4, ATF3, THAP1, CHD7, ZNF532, CBFB, MECOM, SMARCE1, TP63, MITF, MYOG, JMJD1C, TEAD1, TRIM28, ETV1, LMO2, ESR1, OCA2, MLL, CTCF, TCF12, JUN, EP300, NUTM1, MNT, GATA6, PAX8, DPF2, E2F6, RFX5, ZNF528, TEAD4, KMT2B, TFAP2C, EED, GLIS1, POU2F2, CHD8, ZSCAN5D, MYCN, POU5F1, TOP2A, RUNX1T1, ID3, CTBP1, ZNF317, ZNF263, ZBTB48, DUX4, STAT1, SRF, ERG2, TBP, ERG, PBX1, ASCL1, OGG1, ETS1, MYC, EZH1, SMARCA4, ONECUT1, RAD21, GRHL3, GABPA, PRDM14, IKZF1, ZNF398, VDR, NR3C1, CEBPB, ZNF750, KMT2A, CREB1, EZH2, BMPR1A, GRHL2, TRPS1, SPI1, IRF1, HDAC2, INTS13, GATA2, SIX2, FLI1, MXI1, NFIL3, NCOA2, RUNX1, SMC1A, CEBPA, SIRT6, EZH2phosphoT487, SIN3A, ZFX, TET2, ERG3, RARA, ZNF384, CREBBP, ZXDC, RUNX2, CDK6, GATA4, GR, ARNT, NRF1, ATF2, PBX3, FOXM1, CBFA2T3, CDK8, MED1, TEAD3, TERF1, MYB, PIAS1, ZNF3, NCOA1, EVI1, SREBF2, USF1, BCL11A, NIPBL, HNF4A, NR4A1, REST, CTBP2, TCF3, SMC3, STAG1, ZNF394, CBFA2T2, PPARG, AGO1, FOXA2, WT1, ESR2, FOXF1, MEF2C, HOXB13, KDM1A, YY1, RELA, SP140, ZIC2, HIF1A, GATA3, TAL1, MAX, NRIP1, ZNF143, GATA1, CBX2, PLAG1, KLF4, NCOA3, NR2F2, NR2F1, TP53, ZNF334, MYOD1, EGR2, T, AR, ZBTB16, RXR, ZBTB26, HSF1, NCOR1, BRD4, RNF2, JUND, CLOCK, CUX1, MAZ, ZNF24, AHR, FOSL2
- Target gene symbol (double-evidenced CRMs): CFAP410,TRPM2,PFKL,C2CD2,HSF2BP,SLC37A1,PDXK,PKNOX1,TSPEAR,UBASH3A,PDE9A
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 11
- Number of somatic mutations (non-coding): 0
- Related genes and loops
- Related gene:
ENSG00000157617,
ENSG00000160185,
ENSG00000160190,
ENSG00000160191,
ENSG00000160199,
ENSG00000160207,
ENSG00000160209,
ENSG00000141959,
ENSG00000160226,
ENSG00000142185,
ENSG00000175894,
- Related loop:
chr21:41625000-41650000~~chr21:43575000-43600000,
chr21:41925000-41950000~~chr21:43575000-43600000,
chr21:42425000-42450000~~chr21:43575000-43600000,
chr21:42525000-42550000~~chr21:43575000-43600000,
chr21:42575000-42600000~~chr21:43575000-43600000,
chr21:42725000-42750000~~chr21:43575000-43600000,
chr21:42800000-42825000~~chr21:43575000-43600000,
chr21:42925000-42950000~~chr21:43575000-43600000,
chr21:42975000-43000000~~chr21:43575000-43600000,
chr21:43000000-43025000~~chr21:43575000-43600000,
chr21:43175000-43200000~~chr21:43575000-43600000,
chr21:43200000-43225000~~chr21:43575000-43600000,
chr21:43250000-43275000~~chr21:43575000-43600000,
chr21:43300000-43325000~~chr21:43575000-43600000,
chr21:43325000-43350000~~chr21:43575000-43600000,
chr21:43350000-43375000~~chr21:43575000-43600000,
chr21:43575000-43600000~~chr21:43725000-43750000,
chr21:43575000-43600000~~chr21:44325000-44350000,
chr21:43575000-43600000~~chr21:44475000-44500000,
chr21:43575000-43600000~~chr21:44675000-44700000,
chr21:6025000-6050000~~chr21:43575000-43600000,
chr21:6125000-6150000~~chr21:43575000-43600000,
chr21:6425000-6450000~~chr21:43575000-43600000,