Variant report

Variant	rs471231
Chromosome Location	chr12:118187337-118187338
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10850897	0.83[AFR][1000 genomes]
rs477022	0.80[EUR][1000 genomes]
rs481593	0.81[EUR][1000 genomes]
rs510907	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs515398	0.83[EUR][1000 genomes]
rs570592	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs584654	0.81[EUR][1000 genomes]
rs604248	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs614651	0.81[EUR][1000 genomes]
rs61937721	0.86[EUR][1000 genomes]
rs61937724	0.87[EUR][1000 genomes]
rs630460	0.81[EUR][1000 genomes]
rs630808	0.83[EUR][1000 genomes]
rs6490152	0.92[EUR][1000 genomes]
rs665540	0.80[EUR][1000 genomes]
rs675383	0.80[EUR][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs471231	C12orf51	cis	cerebellum	SCAN

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118186600-118187600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr12:118187000-118187600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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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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