Variant report

Variant	rs10126447
Chromosome Location	chrX:104988706-104988707
allele	A/G
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]
rs10218388	0.87[ASW][hapmap];1.00[CEU][hapmap];0.81[GIH][hapmap];0.84[MKK][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	0.86[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][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]
rs210439	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]
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	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	0.87[ASW][hapmap];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];1.00[LWK][hapmap];0.93[MKK][hapmap];0.88[YRI][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:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:104988000-104989200	Weak transcription	Placenta	Placenta
2	chrX:104988000-104990400	Enhancers	NHEK	skin
3	chrX:104988000-104990600	Enhancers	HMEC	breast

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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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