Variant report

Variant	rs7512315
Chromosome Location	chr1:211893655-211893656
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs11119797	0.85[EUR][1000 genomes]
rs11119801	0.99[ASN][1000 genomes]
rs12057678	0.95[ASN][1000 genomes]
rs12123627	0.81[EUR][1000 genomes]
rs12130915	0.89[EUR][1000 genomes]
rs12145195	0.99[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12145981	0.89[EUR][1000 genomes]
rs1773352	0.87[ASN][1000 genomes]
rs56230302	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs61672280	0.95[ASN][1000 genomes]
rs7525086	0.89[EUR][1000 genomes]
rs7543710	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7545954	0.94[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7512315	IL10	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:211879200-211913600	Weak transcription	Right Atrium	heart

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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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