Variant report

Variant	rs16965329
Chromosome Location	chr15:53231847-53231848
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs11070921	0.86[CHB][hapmap]
rs11070935	0.84[ASN][1000 genomes]
rs12101773	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.85[MEX][hapmap];1.00[TSI][hapmap]
rs16965332	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];0.85[MEX][hapmap];0.84[MKK][hapmap];1.00[TSI][hapmap]
rs2120441	1.00[TSI][hapmap]
rs2414215	0.93[ASN][1000 genomes]
rs2456520	0.85[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs61588331	1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs62023539	0.98[ASN][1000 genomes]
rs7176412	1.00[TSI][hapmap]
rs8024111	1.00[CHB][hapmap];0.94[JPT][hapmap]

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	esv2579232	chr15:53230986-53232223	Inactive region	TF binding region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:0 , 50 per page) page:

No data

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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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