Variant report

Variant	rs12283279
Chromosome Location	chr11:32372489-32372490
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10835898	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11031703	1.00[AMR][1000 genomes]
rs11031825	1.00[AMR][1000 genomes]
rs11824202	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11825204	1.00[AMR][1000 genomes]
rs12276632	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12287273	1.00[AMR][1000 genomes]
rs12288783	1.00[AMR][1000 genomes]
rs12294446	1.00[AMR][1000 genomes]
rs5030285	1.00[AMR][1000 genomes]
rs7107141	1.00[AMR][1000 genomes]
rs7936995	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518414	chr11:32371215-32375669	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:32370000-32375000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr11:32370800-32375400	Weak transcription	Colon Smooth Muscle	Colon
3	chr11:32372400-32373800	Weak transcription	Fetal Heart	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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