Variant report

Variant	rs6914525
Chromosome Location	chr6:133988652-133988653
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11961183	0.80[EUR][1000 genomes]
rs12210532	0.81[CHB][hapmap]
rs12661401	0.81[EUR][1000 genomes]
rs13205217	0.81[ASN][1000 genomes]
rs13218156	0.82[EUR][1000 genomes]
rs1468052	0.83[ASN][1000 genomes]
rs1476382	0.83[ASN][1000 genomes]
rs17398008	0.81[CHB][hapmap];0.81[GIH][hapmap]
rs17476396	0.81[CHB][hapmap];0.81[GIH][hapmap]
rs2015084	0.89[AFR][1000 genomes]
rs2207405	0.81[ASN][1000 genomes]
rs2327380	0.86[ASN][1000 genomes]
rs34537042	0.83[ASN][1000 genomes]
rs36055382	0.81[ASN][1000 genomes]
rs4470864	0.89[AFR][1000 genomes]
rs62429273	0.84[EUR][1000 genomes]
rs6569890	0.89[AFR][1000 genomes]
rs6569892	0.99[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6569894	0.99[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs6900835	0.89[AFR][1000 genomes]
rs6900893	0.89[AFR][1000 genomes]
rs6925029	0.80[ASN][1000 genomes]
rs71576327	0.83[ASN][1000 genomes]
rs766996	0.83[ASN][1000 genomes]
rs7738973	0.98[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs7749675	0.82[ASN][1000 genomes]
rs7750428	0.89[AFR][1000 genomes]
rs9483598	0.89[AFR][1000 genomes]
rs9483599	0.86[AFR][1000 genomes]
rs9493685	0.88[AFR][1000 genomes]
rs9493690	0.83[CHB][hapmap];0.81[ASN][1000 genomes]
rs9493692	0.81[ASN][1000 genomes]
rs9493695	0.81[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	nsv1032687	chr6:133987372-134059728	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1024201	chr6:133987372-134062162	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive 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	chr6:133988600-133988800	ZNF genes & repeats	Fetal Lung	lung

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Input of quick search could be:

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

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