Variant report

Variant	rs10821123
Chromosome Location	chr9:96169561-96169562
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10821124	0.81[AMR][1000 genomes]
rs10992716	0.91[ASW][hapmap];0.80[LWK][hapmap];0.90[YRI][hapmap]
rs10992769	0.84[JPT][hapmap]
rs12379660	0.81[CHD][hapmap]
rs13287066	0.91[CHB][hapmap]
rs2100928	0.82[CEU][hapmap];0.84[JPT][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes];0.84[EUR][1000 genomes]
rs4481672	0.81[AMR][1000 genomes]
rs5019496	0.85[AFR][1000 genomes]
rs7870079	0.83[CHB][hapmap];0.94[GIH][hapmap];0.84[MEX][hapmap]
rs944990	0.89[AFR][1000 genomes]

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs10821123	FAM120A	cis	cerebellum	SCAN
rs10821123	CENPP	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96169000-96169800	Enhancers	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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