Variant report

Variant	rs204166
Chromosome Location	chrX:57097325-57097326
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]
rs10521485	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs150099	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2071722	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs378487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs538910	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5914036	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs5914037	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs5914052	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5914874	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs5914897	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs5960235	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]
rs6612746	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs6612757	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs697664	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs707346	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs912956	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:57096400-57117000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chrX:57096800-57097400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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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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