Variant report

Variant	rs5962570
Chromosome Location	chrX:104949120-104949121
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11092543	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap]
rs210427	1.00[JPT][hapmap];0.81[YRI][hapmap]
rs210429	1.00[JPT][hapmap];0.81[YRI][hapmap]
rs210431	0.81[YRI][hapmap]
rs210731	1.00[JPT][hapmap]
rs382243	1.00[JPT][hapmap]
rs400049	1.00[JPT][hapmap]
rs5962297	1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap]
rs5962577	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap]
rs5962578	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap]
rs7063036	1.00[JPT][hapmap]
rs9887672	1.00[CHB][hapmap];0.87[CHD][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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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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