Variant report

Variant	rs9455306
Chromosome Location	chr6:71763083-71763084
allele	A/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]
rs13437398	1.00[EUR][1000 genomes]
rs6916336	1.00[EUR][1000 genomes]
rs732530	1.00[EUR][1000 genomes]
rs7762330	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446331	1.00[EUR][1000 genomes]
rs9446332	1.00[EUR][1000 genomes]
rs9446333	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446335	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9446336	1.00[EUR][1000 genomes]
rs9455307	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9455308	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9455325	1.00[EUR][1000 genomes]
rs9455326	1.00[EUR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:71762000-71763200	Enhancers	Brain Germinal Matrix	brain
2	chr6:71762000-71763600	Enhancers	Fetal Brain Female	brain
3	chr6:71762000-71763800	Enhancers	Fetal Brain Male	brain
4	chr6:71763000-71765800	Weak transcription	Cortex derived primary cultured neurospheres	brain

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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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