Variant report

Variant	rs2063982
Chromosome Location	chr14:78703155-78703156
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs17754913	0.83[CEU][hapmap]
rs17827951	0.83[CEU][hapmap]
rs2063983	0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4903732	0.84[CHB][hapmap];0.81[JPT][hapmap];0.90[ASN][1000 genomes]
rs60670448	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7145062	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7148695	0.83[CEU][hapmap]
rs7161683	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8009477	0.84[CHB][hapmap];0.81[JPT][hapmap];0.90[ASN][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2063982	FOS	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78694200-78706800	Weak transcription	Brain Angular Gyrus	brain
2	chr14:78699400-78714200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr14:78699800-78709000	Weak transcription	Brain Anterior Caudate	brain
4	chr14:78702600-78704000	Weak transcription	Brain Germinal Matrix	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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