Variant report

Variant	rs17093509
Chromosome Location	chr10:117482906-117482907
allele	C/G
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]
rs1034939	0.81[ASN][1000 genomes]
rs1034940	0.81[ASN][1000 genomes]
rs11197423	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17093513	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2255909	0.90[CEU][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2532726	0.82[JPT][hapmap]
rs2804148	0.84[CEU][hapmap]
rs2804153	0.85[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2804155	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2804158	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4491139	0.87[EUR][1000 genomes]
rs4751927	0.82[CHB][hapmap];0.80[JPT][hapmap]
rs7093582	0.80[JPT][hapmap]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:117471000-117490600	Weak transcription	Aorta	Aorta
2	chr10:117480600-117485200	Weak transcription	Pancreatic Islets	Pancreatic Islet

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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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