Variant report

Variant	rs6862014
Chromosome Location	chr5:57501631-57501632
allele	C/T
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]
rs10057511	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16887914	0.83[EUR][1000 genomes]
rs17695268	0.91[JPT][hapmap]
rs2052548	0.91[JPT][hapmap]
rs34139715	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34563011	0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs41445844	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6891097	0.90[CEU][hapmap];0.92[EUR][1000 genomes]
rs6896231	0.81[EUR][1000 genomes]
rs72753380	0.83[EUR][1000 genomes]
rs72753383	0.83[EUR][1000 genomes]
rs72753387	0.85[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:57498400-57505400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr5:57501400-57502600	Weak transcription	Aorta	Aorta

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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