Variant report

Variant	rs1764940
Chromosome Location	chr13:86220061-86220062
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 50 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs1011902	0.83[EUR][1000 genomes]
rs1415396	0.82[EUR][1000 genomes]
rs1538049	0.83[EUR][1000 genomes]
rs1538050	0.83[EUR][1000 genomes]
rs1538051	0.83[EUR][1000 genomes]
rs1538056	0.84[EUR][1000 genomes]
rs1538066	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1556773	0.83[EUR][1000 genomes]
rs1753738	0.86[EUR][1000 genomes]
rs1753741	0.86[EUR][1000 genomes]
rs1753764	0.82[EUR][1000 genomes]
rs1753768	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1753771	0.83[EUR][1000 genomes]
rs1753772	0.83[EUR][1000 genomes]
rs1753773	0.88[ASN][1000 genomes]
rs1753775	0.96[ASN][1000 genomes]
rs1753780	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1753789	0.90[EUR][1000 genomes]
rs1753795	0.86[EUR][1000 genomes]
rs1764951	0.86[EUR][1000 genomes]
rs1764953	0.86[EUR][1000 genomes]
rs1764958	0.83[EUR][1000 genomes]
rs1764959	0.83[EUR][1000 genomes]
rs1764961	0.82[EUR][1000 genomes]
rs1764964	0.83[EUR][1000 genomes]
rs1764968	0.89[EUR][1000 genomes]
rs1764971	0.96[ASN][1000 genomes]
rs1928139	0.83[AFR][1000 genomes]
rs2243633	0.84[EUR][1000 genomes]
rs2245400	0.83[EUR][1000 genomes]
rs2255983	0.84[EUR][1000 genomes]
rs2343058	0.83[EUR][1000 genomes]
rs4542551	0.82[EUR][1000 genomes]
rs4911018	0.83[EUR][1000 genomes]
rs7342473	0.83[EUR][1000 genomes]
rs7982006	0.83[EUR][1000 genomes]
rs9531827	0.83[EUR][1000 genomes]
rs9547325	0.83[EUR][1000 genomes]
rs9547327	0.83[EUR][1000 genomes]
rs9547328	0.83[EUR][1000 genomes]
rs9547334	0.82[EUR][1000 genomes]
rs9602804	0.84[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916866	chr13:85505771-86241562	Active TSS Enhancers Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv2752724	chr13:85810499-86320999	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv1037563	chr13:85830511-86414012	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv471162	chr13:85994700-86296819	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv456051	chr13:85994700-86306452	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv562609	chr13:85994700-86306452	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv428608	chr13:86109178-86262577	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv900733	chr13:86192376-86309366	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:86214400-86225000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:86218400-86220200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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