- Basic information
- CohesinDB ID: CDBP00421087
- Locus: chr21-44723185-44724478
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Data sourse: ENCSR000BLD, GSE206145-GSE177045, GSE67783, GSE86191, GSE116868, GSE111913, GSE105028, GSE206145-NatGen2015, ENCSR000ECE, GSE206145, ENCSR153HNT
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Cell type: MCF-7, H1-hESC, RPE, Fibroblast, HCT-116, MB157, RT-112, K-562, 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): 0.889
- Subunit: Mau2,SA1,Rad21,SMC1
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CTCF binding site: CTCF
CTCF motif: False
- Genomic location: Intergenic
- 3D genome
- TAD boundary: Boundary
- Chromatin hubs: Hub
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Hi-C loops: True
Hi-ChIP loops: True
ChIA-PET loops: True
- Compartment:
80% Hi-C samples shows Compartment A
- Cis-regulatory elements
- Enhancer (Fantom5): non-Enhancer
- Super enhancer (SEdb): False
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Chromatin annotation:
"13_ReprPC": 38%,
"12_EnhBiv": 28%,
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: FOXO1, TRIM25, SUZ12, RING1B, MLL4, ZFHX2, LYL1, BMI1, ATF3, HNRNPUL1, CTCFL, CHD7, THAP1, CBFB, ZNF189, TP63, MITF, JMJD1C, KLF5, TRIM28, LMO2, ESR1, MLL, TP73, OCA2, CTCF, EP300, ARID5B, RYBP, DPF2, E2F6, TRIM24, KMT2B, PDX1, TFAP2C, EED, JARID2, NANOG, CHD8, BRD1, POU2F2, MYCN, POU5F1, ZNF263, KDM4C, ZBTB17, ZBTB48, DDX5, ERG2, ERG, PBX1, OGG1, MYC, SMARCA4, RFX1, KDM4A, RAD21, GRHL3, PROX1, GABPA, STAT3, NKX3-1, PRDM14, IKZF1, RCOR1, DNMT3B, CEBPB, KMT2A, EZH2, SPI1, HDAC2, GATAD2B, MXD3, SIX2, FLI1, SMARCA5, RUNX1, CEBPA, EZH2phosphoT487, NKX2-2, SIRT6, ZFX, ERG3, CBX8, SMARCC1, RARA, PRPF4, NOTCH1, TAF15, MAFB, NCAPH2, CHD1, CDK8, MYB, SCRT2, SETDB1, STAT5A, BCL11A, TFAP2A, POU2F3, ASH2L, CTBP2, BCOR, TCF3, AATF, STAG1, TRP47, CBFA2T2, MEF2B, FOXA2, RBBP5, EBF1, WT1, KDM1A, YY1, RELA, TARDBP, BRG1, SP140, HIF1A, PCGF1, TAL1, MAX, CBX2, PLAG1, NCOA3, NEUROG2, TCF7L2, KDM5B, TP53, PKNOX1, MED, EGR2, T, BHLHE40, AR, RXR, HEXIM1, TFIIIC, HSF1, RNF2, BRD4, SCRT1, MAZ, AHR
- Target gene symbol (double-evidenced CRMs): CFAP410,ITGB2-AS1,TRPM2,TSPEAR,PFKL,GATD3A,ITGB2,FAM207A
- Function elements
- Human SNPs: .
- Number of somatic mutations (coding): 0
- Number of somatic mutations (non-coding): 10
- Related genes and loops
- Related gene:
ENSG00000160221,
ENSG00000141959,
ENSG00000160226,
ENSG00000142185,
ENSG00000175894,
ENSG00000160255,
ENSG00000227039,
ENSG00000160256,
- Related loop:
chr21:43350000-43375000~~chr21:44725000-44750000,
chr21:44075000-44100000~~chr21:44725000-44750000,
chr21:44175000-44200000~~chr21:44700000-44725000,
chr21:44325000-44350000~~chr21:44700000-44725000,
chr21:44325000-44350000~~chr21:44725000-44750000,
chr21:44350000-44375000~~chr21:44725000-44750000,
chr21:44375000-44400000~~chr21:44725000-44750000,
chr21:44475000-44500000~~chr21:44725000-44750000,
chr21:44500000-44525000~~chr21:44700000-44725000,
chr21:44500000-44525000~~chr21:44725000-44750000,
chr21:44509197-44511724~~chr21:44717965-44719686,
chr21:44509213-44512100~~chr21:44718108-44719341,
chr21:44509225-44511899~~chr21:44717741-44719707,
chr21:44509481-44512016~~chr21:44717736-44719579,
chr21:44509926-44511467~~chr21:44718171-44719367,
chr21:44525000-44550000~~chr21:44725000-44750000,
chr21:44575000-44600000~~chr21:44725000-44750000,
chr21:44625000-44650000~~chr21:44725000-44750000,
chr21:44700000-44725000~~chr21:44925000-44950000,