Variant report

Variant	rs67908341
Chromosome Location	chr8:34314898-34314899
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10089410	1.00[ASN][1000 genomes]
rs10092484	1.00[ASN][1000 genomes]
rs10099704	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10099911	1.00[ASN][1000 genomes]
rs10100213	0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10100329	0.82[AMR][1000 genomes]
rs10108508	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10111870	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs10217066	1.00[ASN][1000 genomes]
rs11994160	1.00[ASN][1000 genomes]
rs12334566	1.00[ASN][1000 genomes]
rs16882055	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16882266	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16882365	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16882528	1.00[ASN][1000 genomes]
rs2719272	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28407707	1.00[ASN][1000 genomes]
rs28505609	1.00[ASN][1000 genomes]
rs34005391	1.00[ASN][1000 genomes]
rs34564700	1.00[ASN][1000 genomes]
rs35112066	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6468269	1.00[ASN][1000 genomes]
rs67406212	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6988783	1.00[ASN][1000 genomes]
rs7000467	0.81[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs7009639	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7014310	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs71513723	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72640903	1.00[ASN][1000 genomes]
rs72640915	1.00[ASN][1000 genomes]
rs72640931	1.00[ASN][1000 genomes]
rs72640933	1.00[ASN][1000 genomes]
rs72640961	1.00[ASN][1000 genomes]
rs72640962	1.00[ASN][1000 genomes]
rs7815445	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3421299	chr8:34311710-34315908	Enhancers Flanking Active TSS Active TSS	n/a	n/a	inside rSNPs	diseases
2	nsv6147	chr8:34314029-34359124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34314800-34315200	Enhancers	HUES64 Cell Line	embryonic stem cell

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