Variant report

Variant	rs210432
Chromosome Location	chrX:104947296-104947297
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10126447	0.86[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap]
rs210431	0.83[ASW][hapmap];0.86[CHB][hapmap];0.89[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap]
rs210434	0.86[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap]
rs210439	0.91[ASW][hapmap];0.86[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs210544	0.81[ASW][hapmap]
rs210545	0.81[ASW][hapmap]
rs210550	1.00[ASW][hapmap];0.86[MKK][hapmap];1.00[YRI][hapmap]
rs3764765	0.82[CHD][hapmap];1.00[JPT][hapmap]
rs400000	0.87[GIH][hapmap];0.80[MEX][hapmap]
rs440424	0.81[ASW][hapmap]
rs452428	0.87[GIH][hapmap];0.80[MEX][hapmap]
rs5916932	0.81[ASW][hapmap];0.84[GIH][hapmap];0.80[MEX][hapmap]
rs5962298	0.82[CHD][hapmap];1.00[JPT][hapmap]
rs7891511	0.86[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:104946400-104950200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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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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