Variant report

Variant	rs1050705
Chromosome Location	chrX:154064200-154064201
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs1075950	1.00[CEU][hapmap]
rs1126762	0.89[CHD][hapmap]
rs1470586	0.88[CHD][hapmap]
rs1472977	1.00[ASW][hapmap];1.00[CHB][hapmap];0.82[GIH][hapmap]
rs17051889	0.88[CHD][hapmap]
rs1848762	0.89[CHD][hapmap]
rs1936645	1.00[CEU][hapmap];0.88[CHB][hapmap]
rs2096362	1.00[CEU][hapmap];0.89[CHD][hapmap];0.81[GIH][hapmap];0.88[MEX][hapmap]
rs2221730	0.89[CHD][hapmap]
rs2664161	1.00[ASW][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap]
rs2728538	0.88[CHB][hapmap];0.94[CHD][hapmap]
rs4074307	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];0.95[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.95[TSI][hapmap];0.82[YRI][hapmap]
rs4898352	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.91[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs4898396	0.89[CHD][hapmap]
rs5945250	1.00[CHB][hapmap];1.00[CHD][hapmap];0.88[GIH][hapmap]
rs5987077	1.00[CEU][hapmap];0.89[CHD][hapmap];0.81[GIH][hapmap];0.94[MEX][hapmap]
rs5987079	1.00[CEU][hapmap];0.89[CHD][hapmap];0.81[GIH][hapmap];0.88[MEX][hapmap]
rs6643622	0.88[CHB][hapmap];1.00[CHD][hapmap];1.00[LWK][hapmap];0.89[MEX][hapmap];1.00[YRI][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:154064000-154064800	Enhancers	K562	blood

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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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