Variant report

Variant	rs73434487
Chromosome Location	chr6:54876766-54876767
allele	G/T
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]
rs16886099	1.00[EUR][1000 genomes]
rs3105260	1.00[EUR][1000 genomes]
rs57915824	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58658626	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59536488	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59630560	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6923998	1.00[EUR][1000 genomes]
rs73438551	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73438552	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73438561	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7356813	1.00[EUR][1000 genomes]
rs7740224	1.00[EUR][1000 genomes]
rs7762218	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7766442	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9475055	1.00[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:54876600-54876800	Enhancers	Skeletal Muscle Male	skeletal muscle
2	chr6:54876600-54877000	Enhancers	Fetal Lung	lung
3	chr6:54876600-54877600	Enhancers	Placenta Amnion	Placenta Amnion

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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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