Variant report

Variant	rs7607357
Chromosome Location	chr2:168015952-168015953
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10497310	0.91[JPT][hapmap];0.86[MEX][hapmap];0.82[ASN][1000 genomes]
rs12104632	1.00[CEU][hapmap]
rs16852938	1.00[CEU][hapmap];0.83[GIH][hapmap]
rs16853051	1.00[JPT][hapmap];0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs16853061	0.91[JPT][hapmap]
rs16853195	1.00[CEU][hapmap];0.95[GIH][hapmap];0.83[TSI][hapmap]
rs2303877	0.81[ASW][hapmap];1.00[CEU][hapmap];0.91[GIH][hapmap]
rs61661888	0.84[ASN][1000 genomes]
rs6432978	1.00[CEU][hapmap];0.86[GIH][hapmap]
rs73025703	0.84[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	nsv875376	chr2:167844513-168037489	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	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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