Variant report

Variant	rs9568342
Chromosome Location	chr13:50441690-50441691
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11618972	0.94[ASN][1000 genomes]
rs2407706	0.87[ASN][1000 genomes]
rs4548769	0.80[EUR][1000 genomes]
rs4942887	0.96[ASN][1000 genomes]
rs55684391	0.94[ASN][1000 genomes]
rs7139851	0.96[ASN][1000 genomes]
rs7983607	0.99[ASN][1000 genomes]
rs9526613	0.96[ASN][1000 genomes]
rs9526615	0.98[ASN][1000 genomes]
rs9535384	0.96[ASN][1000 genomes]
rs9535385	0.96[ASN][1000 genomes]
rs9535387	1.00[ASN][1000 genomes]
rs9568339	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9568340	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9568341	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9568342	DLEU2///DLEU2L	trans	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:50434200-50442000	Weak transcription	Pancreas	Pancrea

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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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