Variant report

Variant	rs10208045
Chromosome Location	chr2:191256032-191256033
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs10170897	0.82[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs10190016	0.85[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs10202825	0.87[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs13390311	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13409203	0.91[AFR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34121676	0.81[ASN][1000 genomes]
rs73048070	0.97[ASN][1000 genomes]
rs73050047	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3410695	chr2:191255814-191256321	Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:191256000-191256400	Enhancers	K562	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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