Variant report

Variant	rs2866168
Chromosome Location	chr4:100657673-100657674
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10516453	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13123292	0.83[AMR][1000 genomes]
rs1491242	0.86[EUR][1000 genomes]
rs17029292	1.00[CEU][hapmap]
rs17608848	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs34849574	1.00[ASN][1000 genomes]
rs3828542	0.88[CEU][hapmap]
rs4699759	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs56184565	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6532828	0.83[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6858032	1.00[CEU][hapmap]
rs6858700	1.00[CEU][hapmap]

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs2866168	MANBA	cis	cerebellum	SCAN
rs2866168	EMCN	cis	parietal	SCAN
rs2866168	H2AFZ	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100656800-100658200	Enhancers	Skeletal Muscle Male	skeletal muscle

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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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