Variant report

Variant	rs703352
Chromosome Location	chr10:117146337-117146338
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10787567	0.87[ASN][1000 genomes]
rs11197173	0.87[ASN][1000 genomes]
rs12253499	0.81[ASN][1000 genomes]
rs1494174	0.89[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs1565833	0.92[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2201363	0.80[ASN][1000 genomes]
rs2485966	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs2485968	0.89[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs2485971	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs594160	0.89[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs615905	0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs671943	0.81[ASN][1000 genomes]
rs675816	0.88[ASN][1000 genomes]
rs683117	0.82[AMR][1000 genomes];0.90[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117138200-117150800	Weak transcription	Aorta	Aorta
2	chr10:117145400-117146600	Weak transcription	iPS-15b 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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