Variant report

Variant	rs7085674
Chromosome Location	chr10:23686735-23686736
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11013427	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11013432	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11013433	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56984761	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57142582	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7077959	1.00[EUR][1000 genomes]
rs7078402	1.00[EUR][1000 genomes]
rs7101025	1.00[EUR][1000 genomes]
rs73602541	1.00[EUR][1000 genomes]
rs73602543	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73602544	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73602547	1.00[EUR][1000 genomes]
rs73602571	1.00[EUR][1000 genomes]
rs7921695	1.00[EUR][1000 genomes]
rs9651373	1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:23684800-23688800	Enhancers	Stomach Mucosa	stomach
2	chr10:23686600-23687400	Weak transcription	Placenta	Placenta

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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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