Variant report

Variant	rs210439
Chromosome Location	chrX:104959059-104959060
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10126447	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs10218388	1.00[CEU][hapmap];0.81[GIH][hapmap];1.00[TSI][hapmap]
rs11092543	1.00[CEU][hapmap];0.92[TSI][hapmap]
rs210431	0.82[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap]
rs210432	0.91[ASW][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs210434	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs210550	0.91[ASW][hapmap];1.00[YRI][hapmap]
rs3764765	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs5962297	1.00[CEU][hapmap];0.92[TSI][hapmap]
rs5962298	0.83[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs5962575	1.00[CEU][hapmap];0.81[GIH][hapmap];1.00[TSI][hapmap]
rs5962577	1.00[CEU][hapmap];0.92[TSI][hapmap]
rs5962578	1.00[CEU][hapmap]
rs7063036	0.82[ASW][hapmap]
rs7891511	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs9887672	1.00[CEU][hapmap];0.92[TSI][hapmap]

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:104955200-104961600	Enhancers	Placenta	Placenta

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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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