Variant report

Variant	rs10976928
Chromosome Location	chr9:8301307-8301308
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10115782	0.89[CEU][hapmap];1.00[JPT][hapmap]
rs10125894	1.00[JPT][hapmap]
rs10758962	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs10815820	0.90[ASN][1000 genomes]
rs10815824	0.90[ASN][1000 genomes]
rs10815825	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10815835	1.00[JPT][hapmap]
rs10815836	1.00[JPT][hapmap]
rs10815837	1.00[JPT][hapmap]
rs10815838	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs10976929	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10976937	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10976939	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10976940	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10976941	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10976942	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10976949	0.90[ASN][1000 genomes]
rs10976951	0.90[ASN][1000 genomes]
rs10976955	0.84[ASN][1000 genomes]
rs10976964	0.81[ASN][1000 genomes]
rs10976971	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10976972	0.81[CEU][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10976973	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10976977	0.91[CEU][hapmap];0.86[JPT][hapmap]
rs10976979	0.90[ASN][1000 genomes]
rs10976982	0.90[ASN][1000 genomes]
rs10976984	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10976994	0.90[CEU][hapmap];1.00[JPT][hapmap]
rs10976996	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs10976997	0.87[CEU][hapmap];1.00[JPT][hapmap]
rs10976999	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs10977002	1.00[JPT][hapmap]
rs10977003	1.00[JPT][hapmap]
rs10977004	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs10977013	1.00[JPT][hapmap]
rs10977015	1.00[JPT][hapmap]
rs11532964	0.80[ASN][1000 genomes]
rs11535417	0.84[ASN][1000 genomes]
rs11535419	0.80[ASN][1000 genomes]
rs11536769	0.90[ASN][1000 genomes]
rs11560544	0.84[ASN][1000 genomes]
rs11560545	0.84[ASN][1000 genomes]
rs11562287	0.84[ASN][1000 genomes]
rs12057000	1.00[JPT][hapmap]
rs12236853	0.81[ASN][1000 genomes]
rs12237491	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12238522	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16924671	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16924677	0.81[ASN][1000 genomes]
rs3736380	0.90[ASN][1000 genomes]
rs3847286	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs56370724	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56964282	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59843495	1.00[ASN][1000 genomes]
rs61523941	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7033209	0.91[EUR][1000 genomes]
rs7033267	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs73640802	0.91[EUR][1000 genomes]
rs73643603	0.91[EUR][1000 genomes]
rs73643607	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73643608	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73643609	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73643610	0.84[ASN][1000 genomes]
rs73643611	0.90[ASN][1000 genomes]
rs7868317	0.81[ASN][1000 genomes]
rs7875563	0.90[CEU][hapmap]
rs995336	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv8414	chr9:7827373-8511613	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1016723	chr9:8223541-8303017	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
3	nsv1031472	chr9:8250901-8712547	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv892223	chr9:8258921-8318948	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS	miRNA target site	n/a	inside rSNPs	diseases
5	nsv892224	chr9:8263737-8338431	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS	miRNA target site	n/a	inside rSNPs	diseases
6	esv2762787	chr9:8282283-8310704	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
7	esv3337718	chr9:8301001-8318939	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	miRNA target site	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:8301200-8301600	Enhancers	HUVEC	blood vessel

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links