Variant report

Variant	rs12665148
Chromosome Location	chr6:144443023-144443024
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11751524	0.90[CHB][hapmap];0.90[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11752662	0.91[JPT][hapmap];1.00[EUR][1000 genomes]
rs11753175	1.00[EUR][1000 genomes]
rs11753428	1.00[EUR][1000 genomes]
rs11754802	1.00[EUR][1000 genomes]
rs11755758	0.91[JPT][hapmap];1.00[EUR][1000 genomes]
rs11755974	1.00[EUR][1000 genomes]
rs11758098	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11758344	1.00[EUR][1000 genomes]
rs11759466	1.00[EUR][1000 genomes]
rs11760032	1.00[EUR][1000 genomes]
rs17073312	1.00[EUR][1000 genomes]
rs56735264	1.00[EUR][1000 genomes]
rs57325163	1.00[EUR][1000 genomes]
rs58989946	1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144442000-144444000	Weak transcription	Primary hematopoietic stem cells	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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