Variant report

Variant	rs9564623
Chromosome Location	chr13:70395313-70395314
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs11148828	0.95[JPT][hapmap]
rs11618330	0.94[JPT][hapmap]
rs11618357	0.94[JPT][hapmap]
rs11619836	0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs12430131	0.95[JPT][hapmap]
rs12583014	0.95[JPT][hapmap];0.89[ASN][1000 genomes]
rs12584126	0.88[JPT][hapmap]
rs12584317	0.94[JPT][hapmap]
rs1593176	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs1593177	0.83[JPT][hapmap]
rs17085396	0.94[JPT][hapmap]
rs17727950	0.88[JPT][hapmap];0.87[ASN][1000 genomes]
rs17728004	0.94[JPT][hapmap]
rs17728354	0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs17794771	0.94[JPT][hapmap]
rs1890045	0.94[JPT][hapmap]
rs2059299	0.94[JPT][hapmap]
rs2325234	0.94[JPT][hapmap]
rs4304920	0.82[JPT][hapmap]
rs4344608	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57713566	0.88[ASN][1000 genomes]
rs60137040	0.89[ASN][1000 genomes]
rs67089042	0.87[ASN][1000 genomes]
rs67848439	0.87[ASN][1000 genomes]
rs67934724	0.87[ASN][1000 genomes]
rs73210502	0.89[ASN][1000 genomes]
rs73212516	0.86[ASN][1000 genomes]
rs73212517	0.80[ASN][1000 genomes]
rs7986686	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs7987637	0.95[JPT][hapmap]
rs7987960	0.95[JPT][hapmap]
rs7988385	0.94[JPT][hapmap]
rs7992119	0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs9317844	0.95[JPT][hapmap]
rs9317845	0.94[JPT][hapmap]
rs9529646	1.00[JPT][hapmap]
rs9564595	0.84[JPT][hapmap]
rs9564597	0.83[JPT][hapmap]
rs9564604	0.95[JPT][hapmap]
rs9564607	0.94[JPT][hapmap]
rs9564608	0.94[JPT][hapmap]
rs9564609	0.95[JPT][hapmap]
rs9564610	0.94[JPT][hapmap]
rs9564614	0.83[CHB][hapmap];0.94[JPT][hapmap]
rs9564618	0.94[JPT][hapmap];0.89[ASN][1000 genomes]
rs9564619	0.84[JPT][hapmap];0.88[ASN][1000 genomes]
rs9564620	0.87[ASN][1000 genomes]
rs9572262	0.94[JPT][hapmap]
rs9572268	0.89[JPT][hapmap]
rs9572272	0.83[CEU][hapmap];0.94[JPT][hapmap]
rs9572273	0.84[JPT][hapmap]
rs9572284	0.95[JPT][hapmap]
rs9572285	0.94[JPT][hapmap]
rs9572286	0.94[JPT][hapmap]
rs9572287	0.94[JPT][hapmap]
rs9572288	1.00[JPT][hapmap]
rs9572289	0.95[JPT][hapmap]
rs9572291	0.89[JPT][hapmap]
rs9572294	0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9572295	0.94[JPT][hapmap];0.87[ASN][1000 genomes]
rs9634958	0.86[ASN][1000 genomes]
rs9634959	0.87[ASN][1000 genomes]
rs9634960	0.87[ASN][1000 genomes]
rs993138	0.86[ASN][1000 genomes]
rs993139	0.95[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs993140	0.94[ASN][1000 genomes]
rs993141	0.83[CHB][hapmap];0.93[JPT][hapmap];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045844	chr13:70038096-70405435	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv900481	chr13:70147851-70560731	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1054554	chr13:70159715-70502956	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv1837120	chr13:70209507-70425056	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv482460	chr13:70240630-70419347	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	nsv900483	chr13:70254555-70464234	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv900486	chr13:70302991-70421896	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv832643	chr13:70324440-70486661	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	nsv900487	chr13:70327693-70548643	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
10	nsv1041207	chr13:70347748-70473605	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
11	nsv530724	chr13:70393680-71164323	Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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