Variant report

Variant	rs9349250
Chromosome Location	chr6:12514092-12514093
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs13199416	0.91[MEX][hapmap]
rs13211009	0.91[MEX][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs13214038	0.85[CEU][hapmap];0.89[EUR][1000 genomes]
rs13214464	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13217076	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs1413513	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1931548	0.81[CEU][hapmap];0.88[CHD][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap]
rs35802624	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4714632	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7756687	0.91[EUR][1000 genomes]
rs9349245	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9381224	0.85[AMR][1000 genomes];0.81[EUR][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	nsv970077	chr6:12514065-12515389	Inactive region	TF binding region CpG island	1 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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