Variant report

Variant	rs7316094
Chromosome Location	chr12:26299648-26299649
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1466465	1.00[AMR][1000 genomes]
rs1466466	1.00[AMR][1000 genomes]
rs1480041	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1480042	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1600517	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1600518	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2729648	1.00[AMR][1000 genomes]
rs4963964	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4963967	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6487534	0.85[AFR][1000 genomes]
rs6487535	1.00[AMR][1000 genomes]
rs7304897	1.00[AMR][1000 genomes]
rs7959650	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:26288600-26306600	Weak transcription	Aorta	Aorta

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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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