Variant report

Variant	rs1480167
Chromosome Location	chr8:118579460-118579461
allele	C/T
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]
rs11995038	0.86[ASN][1000 genomes]
rs16889881	0.84[AFR][1000 genomes]
rs17667932	0.85[JPT][hapmap]
rs3886841	0.83[EUR][1000 genomes]
rs55663437	0.95[ASN][1000 genomes]
rs62521211	0.81[ASN][1000 genomes]
rs62521230	0.95[ASN][1000 genomes]
rs62521237	0.86[ASN][1000 genomes]
rs6993408	0.85[JPT][hapmap]
rs7003883	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72672167	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs72672168	0.84[EUR][1000 genomes]

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs1480167	NOV	cis	cerebellum	SCAN
rs1480167	MAL2	cis	cerebellum	SCAN
rs1480167	MTBP	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:118579000-118579600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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