Variant report

Variant	rs716225
Chromosome Location	chr8:34146302-34146303
allele	A/G
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]
rs10503958	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1562183	0.95[ASN][1000 genomes]
rs16882013	0.97[ASN][1000 genomes]
rs16882016	0.97[ASN][1000 genomes]
rs16882072	0.93[ASN][1000 genomes]
rs16882098	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4289807	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4739475	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4739543	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60730442	0.95[ASN][1000 genomes]
rs73674310	0.99[ASN][1000 genomes]
rs73674323	0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:34142600-34146800	Weak transcription	Brain Germinal Matrix	brain
2	chr8:34144800-34149200	Enhancers	Fetal Brain Male	brain
3	chr8:34146200-34148000	Enhancers	Fetal Brain Female	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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