Variant report

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1031786	1.00[ASN][1000 genomes]
rs10498570	1.00[ASN][1000 genomes]
rs12432517	1.00[ASN][1000 genomes]
rs12434328	1.00[ASN][1000 genomes]
rs12434420	1.00[ASN][1000 genomes]
rs12435245	1.00[ASN][1000 genomes]
rs12879379	0.96[AFR][1000 genomes]
rs12882862	1.00[ASN][1000 genomes]
rs12885704	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs12887939	1.00[ASN][1000 genomes]
rs17119756	0.84[CEU][hapmap];0.81[YRI][hapmap]
rs17623851	1.00[ASN][1000 genomes]
rs17624978	1.00[ASN][1000 genomes]
rs17625091	1.00[ASN][1000 genomes]
rs17625864	0.84[CEU][hapmap]
rs17654422	1.00[ASN][1000 genomes]
rs17696913	1.00[ASN][1000 genomes]
rs17697055	1.00[ASN][1000 genomes]
rs17703593	1.00[ASN][1000 genomes]
rs34091992	1.00[ASN][1000 genomes]
rs34339499	1.00[ASN][1000 genomes]
rs34354494	1.00[ASN][1000 genomes]
rs35881988	1.00[ASN][1000 genomes]
rs35941036	1.00[ASN][1000 genomes]
rs66752331	1.00[ASN][1000 genomes]
rs7142799	0.84[CEU][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes]
rs7145578	1.00[ASN][1000 genomes]
rs7146489	1.00[ASN][1000 genomes]
rs7150766	1.00[ASN][1000 genomes]
rs8008493	1.00[ASN][1000 genomes]
rs8010059	1.00[ASN][1000 genomes]
rs8018323	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv565376	chr14:84612088-84644822	Enhancers Weak transcription	TF binding region lncRNA	3 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	chr14:84632600-84634800	Enhancers	Fetal Heart	heart

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